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	Gene summary
	Gene structures and expression levels
	Exon skipping events with PSIs in TCGA
	Exon skipping events with PSIs in GTEx
	Open reading frame (ORF) annotation in the exon skipping event
	Exon skipping events in the canonical protein sequence
	SNVs in the skipped exons with depth of coverage
	Splicing Quantitative Trait Loci (sQTLs) in the skipped exons
	Splicing Quantitative Trait Methylation (sQTM) in the skipped exon
	Related drugs with this gene
	Related diseases with this gene

Gene summary for ATXN2L

Gene summary

Gene information	Gene symbol	ATXN2L
	Gene ID	11273
	Gene name	ataxin 2 like
	Synonyms	A2D|A2LG|A2LP|A2RP
	Cytomap	16p11.2
	Type of gene	protein-coding
	Description	ataxin-2-like proteinataxin 2 related proteinataxin-2 domain protein
	Modification date	20180523
	UniProtAcc	Q8WWM7
	Context	PubMed: ATXN2L [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract] - Title (PMID)

Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez

Gene	GO ID	GO term	PubMed ID
ATXN2L	GO:0010603	regulation of cytoplasmic mRNA processing body assembly	23209657

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Exon skipping events across known transcript of Ensembl for ATXN2L from UCSC genome browser

Skipped exons in TCGA and GTEx based on Ensembl gene isoform structure. * Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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Gene isoform structures and expression levels for ATXN2L

Expression levels of gene isoforms across TCGA.

Expression levels of gene isoforms across GTEx.

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Exon skipping events with PSIs in TCGA for ATXN2L

Information of exkip skipping event in TCGA.

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_135070	16	28834802:28834879:28836686:28836723:28836944:28837001	28836686:28836723	ENSG00000168488.14	ENST00000325215.6,ENST00000564304.1,ENST00000382686.4,ENST00000395547.2,ENST00000562867.1,ENST00000336783.4,ENST00000340394.8,ENST00000570200.1
exon_skip_135072	16	28835458:28835863:28836686:28836723:28836944:28837001	28836686:28836723	ENSG00000168488.14	ENST00000568266.1
exon_skip_135076	16	28837560:28837711:28838182:28838307:28840721:28840813	28838182:28838307	ENSG00000168488.14	ENST00000325215.6,ENST00000564304.1,ENST00000382686.4,ENST00000395547.2,ENST00000336783.4,ENST00000340394.8,ENST00000568266.1,ENST00000563314.1,ENST00000570200.1
exon_skip_135077	16	28841935:28842111:28842282:28842393:28843525:28843669	28842282:28842393	ENSG00000168488.14	ENST00000325215.6,ENST00000382686.4,ENST00000395547.2,ENST00000336783.4,ENST00000340394.8,ENST00000563314.1,ENST00000570200.1
exon_skip_135078	16	28841935:28842111:28842305:28842393:28843525:28843669	28842305:28842393	ENSG00000168488.14	ENST00000570284.1
exon_skip_135085	16	28843525:28843720:28843816:28843888:28844137:28844208	28843816:28843888	ENSG00000168488.14	ENST00000325215.6,ENST00000564304.1,ENST00000382686.4,ENST00000395547.2,ENST00000336783.4,ENST00000340394.8,ENST00000563314.1,ENST00000570200.1
exon_skip_135094	16	28843836:28843888:28844137:28844208:28844379:28844675	28844137:28844208	ENSG00000168488.14	ENST00000325215.6,ENST00000564304.1,ENST00000382686.4,ENST00000395547.2,ENST00000336783.4,ENST00000340394.8,ENST00000563314.1,ENST00000570200.1
exon_skip_135100	16	28844516:28844675:28844759:28844829:28845385:28845532	28844759:28844829	ENSG00000168488.14	ENST00000325215.6,ENST00000565845.1,ENST00000564304.1,ENST00000382686.4,ENST00000395547.2,ENST00000565971.1,ENST00000336783.4,ENST00000340394.8,ENST00000563314.1,ENST00000570200.1
exon_skip_135105	16	28846419:28846508:28846598:28846720:28846866:28847079	28846598:28846720	ENSG00000168488.14	ENST00000566946.1
exon_skip_135106	16	28846419:28846508:28846598:28846720:28846869:28847079	28846598:28846720	ENSG00000168488.14	ENST00000325215.6,ENST00000562583.1,ENST00000564304.1,ENST00000382686.4,ENST00000395547.2,ENST00000565971.1,ENST00000336783.4,ENST00000340394.8,ENST00000570200.1
exon_skip_135111	16	28846989:28847079:28847253:28847443:28848048:28848240	28847253:28847443	ENSG00000168488.14	ENST00000340394.8
exon_skip_135112	16	28846989:28847079:28847253:28847497:28848048:28848240	28847253:28847497	ENSG00000168488.14	ENST00000564304.1,ENST00000570200.1
exon_skip_135114	16	28846989:28847079:28847253:28847806:28848048:28848240	28847253:28847806	ENSG00000168488.14	ENST00000562583.1
exon_skip_135139	16	28847443:28847497:28847646:28847811:28848048:28848240	28847646:28847811	ENSG00000168488.14	ENST00000395547.2

PSI values of skipped exons in TCGA.

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Exon skipping events with PSIs in GTEx for ATXN2L

Information of exkip skipping event in GTEx

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_135070	16	28834802:28834879:28836686:28836723:28836944:28837001	28836686:28836723	ENSG00000168488.14	ENST00000340394.8,ENST00000325215.6,ENST00000395547.2,ENST00000336783.4,ENST00000382686.4,ENST00000564304.1,ENST00000570200.1,ENST00000562867.1
exon_skip_135072	16	28835458:28835863:28836686:28836723:28836944:28837001	28836686:28836723	ENSG00000168488.14	ENST00000568266.1
exon_skip_135076	16	28837560:28837711:28838182:28838307:28840721:28840813	28838182:28838307	ENSG00000168488.14	ENST00000563314.1,ENST00000340394.8,ENST00000325215.6,ENST00000395547.2,ENST00000336783.4,ENST00000382686.4,ENST00000564304.1,ENST00000570200.1,ENST00000568266.1
exon_skip_135077	16	28841935:28842111:28842282:28842393:28843525:28843669	28842282:28842393	ENSG00000168488.14	ENST00000563314.1,ENST00000340394.8,ENST00000325215.6,ENST00000395547.2,ENST00000336783.4,ENST00000382686.4,ENST00000570200.1
exon_skip_135078	16	28841935:28842111:28842305:28842393:28843525:28843669	28842305:28842393	ENSG00000168488.14	ENST00000570284.1
exon_skip_135085	16	28843525:28843720:28843816:28843888:28844137:28844208	28843816:28843888	ENSG00000168488.14	ENST00000563314.1,ENST00000340394.8,ENST00000325215.6,ENST00000395547.2,ENST00000336783.4,ENST00000382686.4,ENST00000564304.1,ENST00000570200.1
exon_skip_135094	16	28843836:28843888:28844137:28844208:28844379:28844675	28844137:28844208	ENSG00000168488.14	ENST00000563314.1,ENST00000340394.8,ENST00000325215.6,ENST00000395547.2,ENST00000336783.4,ENST00000382686.4,ENST00000564304.1,ENST00000570200.1
exon_skip_135100	16	28844516:28844675:28844759:28844829:28845385:28845532	28844759:28844829	ENSG00000168488.14	ENST00000563314.1,ENST00000340394.8,ENST00000325215.6,ENST00000395547.2,ENST00000336783.4,ENST00000382686.4,ENST00000564304.1,ENST00000570200.1,ENST00000565971.1,ENST00000565845.1
exon_skip_135105	16	28846419:28846508:28846598:28846720:28846866:28847079	28846598:28846720	ENSG00000168488.14	ENST00000566946.1
exon_skip_135106	16	28846419:28846508:28846598:28846720:28846869:28847079	28846598:28846720	ENSG00000168488.14	ENST00000340394.8,ENST00000325215.6,ENST00000395547.2,ENST00000336783.4,ENST00000382686.4,ENST00000564304.1,ENST00000570200.1,ENST00000565971.1,ENST00000562583.1
exon_skip_135111	16	28846989:28847079:28847253:28847443:28848048:28848240	28847253:28847443	ENSG00000168488.14	ENST00000340394.8
exon_skip_135112	16	28846989:28847079:28847253:28847497:28848048:28848240	28847253:28847497	ENSG00000168488.14	ENST00000564304.1,ENST00000570200.1
exon_skip_135114	16	28846989:28847079:28847253:28847806:28848048:28848240	28847253:28847806	ENSG00000168488.14	ENST00000562583.1
exon_skip_135139	16	28847443:28847497:28847646:28847811:28848048:28848240	28847646:28847811	ENSG00000168488.14	ENST00000395547.2

PSI values of skipped exons in GTEx.

* Skipped exon sequences.

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Open reading frame (ORF) annotation in the exon skipping event for ATXN2L

Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms.

ENST	Start of skipped exon	End of skipped exon	ORF
ENST00000336783	28836686	28836723	Frame-shift
ENST00000336783	28838182	28838307	Frame-shift
ENST00000336783	28844137	28844208	Frame-shift
ENST00000336783	28844759	28844829	Frame-shift
ENST00000336783	28846598	28846720	Frame-shift
ENST00000336783	28842282	28842393	In-frame
ENST00000336783	28843816	28843888	In-frame

Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms.

ENST	Start of skipped exon	End of skipped exon	ORF
ENST00000336783	28836686	28836723	Frame-shift
ENST00000336783	28838182	28838307	Frame-shift
ENST00000336783	28844137	28844208	Frame-shift
ENST00000336783	28844759	28844829	Frame-shift
ENST00000336783	28846598	28846720	Frame-shift
ENST00000336783	28842282	28842393	In-frame
ENST00000336783	28843816	28843888	In-frame

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Infer the effects of exon skipping event on protein functional features for ATXN2L

Exon skipping at the protein sequence level and followed lost functional features. * Click on the image to enlarge it in a new window.

Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases.

ENST	Length of mRNA	Length of AA seq.	Genomic start	Genomic end	mRNA start	mRNA end	AA start	AA end
ENST00000336783	4384	1075	28842282	28842393	1378	1488	403	440
ENST00000336783	4384	1075	28843816	28843888	1684	1755	505	529

Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases.

ENST	Length of mRNA	Length of AA seq.	Genomic start	Genomic end	mRNA start	mRNA end	AA start	AA end
ENST00000336783	4384	1075	28842282	28842393	1378	1488	403	440
ENST00000336783	4384	1075	28843816	28843888	1684	1755	505	529

Lost protein functional features of individual exon skipping events in TCGA.

UniProt acc.

Start of exon skipping (AA)

End of exon skipping (AA)

Protein feature start (AA)

Protein feature end (AA)

Category of protein feature

Description of feature

Lost protein functional features of individual exon skipping events in GTEx.

UniProt acc.

Start of exon skipping (AA)

End of exon skipping (AA)

Protein feature start (AA)

Protein feature end (AA)

Category of protein feature

Description of feature

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SNVs in the skipped exons for ATXN2L

- Lollipop plot for presenting exon skipping associated SNVs. * Click on the image to enlarge it in a new window.

- Differential PSIs between mutated versus non-mutated samples.

ATXN2L_COAD_exon_skip_135085_psi_boxplot.png

ATXN2L_COAD_exon_skip_135111_psi_boxplot.png

ATXN2L_COAD_exon_skip_135112_psi_boxplot.png

ATXN2L_COAD_exon_skip_135114_psi_boxplot.png

ATXN2L_HNSC_exon_skip_135111_psi_boxplot.png

ATXN2L_HNSC_exon_skip_135112_psi_boxplot.png

ATXN2L_HNSC_exon_skip_135114_psi_boxplot.png

ATXN2L_KIRC_exon_skip_135111_psi_boxplot.png

ATXN2L_KIRC_exon_skip_135114_psi_boxplot.png

ATXN2L_LUSC_exon_skip_135114_psi_boxplot.png

ATXN2L_READ_exon_skip_135111_psi_boxplot.png

ATXN2L_READ_exon_skip_135114_psi_boxplot.png

ATXN2L_STAD_exon_skip_135111_psi_boxplot.png

ATXN2L_STAD_exon_skip_135112_psi_boxplot.png

ATXN2L_STAD_exon_skip_135114_psi_boxplot.png

- Non-synonymous mutations located in the skipped exons in TCGA.

Cancer type	Sample	ESID	Skipped exon start	Skipped exon end	Mutation start	Mutation end	Mutation type	Reference seq	Mutation seq	AAchange
LIHC	TCGA-G3-A3CJ-01	exon_skip_135076	28838183	28838307	28838262	28838262	Frame_Shift_Del	G	-	p.E232fs
STAD	TCGA-BR-8487-01	exon_skip_135076	28838183	28838307	28838262	28838262	Frame_Shift_Del	G	-	p.E232fs
UCEC	TCGA-D1-A17M-01	exon_skip_135076	28838183	28838307	28838262	28838262	Frame_Shift_Del	G	-	p.E232fs
ACC	TCGA-OR-A5J5-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
ACC	TCGA-OR-A5J5-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
ACC	TCGA-OR-A5J5-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
ACC	TCGA-OR-A5J5-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
ACC	TCGA-OR-A5J5-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
ACC	TCGA-OR-A5J5-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
COAD	TCGA-AA-3492-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
COAD	TCGA-AA-3492-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
COAD	TCGA-AA-3492-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
HNSC	TCGA-QK-A6VB-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
HNSC	TCGA-QK-A6VB-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
HNSC	TCGA-QK-A6VB-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
READ	TCGA-EI-6882-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
READ	TCGA-EI-6882-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
READ	TCGA-EI-6882-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-6566-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-6566-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-6566-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-8078-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-8078-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-8078-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-8372-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-8372-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-BR-8372-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-CD-A4MI-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-CD-A4MI-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
STAD	TCGA-CD-A4MI-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.H997fs
UCEC	TCGA-A5-A0GH-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
UCEC	TCGA-A5-A0GH-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
UCEC	TCGA-A5-A0GH-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
UCEC	TCGA-BG-A0LX-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
UCEC	TCGA-BG-A0LX-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
UCEC	TCGA-BG-A0LX-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
UCEC	TCGA-D1-A17U-01	exon_skip_135111	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
UCEC	TCGA-D1-A17U-01	exon_skip_135112	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
UCEC	TCGA-D1-A17U-01	exon_skip_135114	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G998fs
COAD	TCGA-AZ-6598-01	exon_skip_135111	28847254	28847443	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
COAD	TCGA-AZ-6598-01	exon_skip_135112	28847254	28847497	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
COAD	TCGA-AZ-6598-01	exon_skip_135114	28847254	28847806	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
STAD	TCGA-BR-7703-01	exon_skip_135111	28847254	28847443	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
STAD	TCGA-BR-7703-01	exon_skip_135112	28847254	28847497	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
STAD	TCGA-BR-7703-01	exon_skip_135114	28847254	28847806	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
STAD	TCGA-BR-8372-01	exon_skip_135111	28847254	28847443	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
STAD	TCGA-BR-8372-01	exon_skip_135112	28847254	28847497	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
STAD	TCGA-BR-8372-01	exon_skip_135114	28847254	28847806	28847356	28847356	Frame_Shift_Del	C	-	p.G999fs
KIRC	TCGA-B0-5092-01	exon_skip_135111	28847254	28847443	28847383	28847383	Frame_Shift_Del	G	-	p.G1009fs
KIRC	TCGA-B0-5092-01	exon_skip_135111	28847254	28847443	28847383	28847383	Frame_Shift_Del	G	-	p.S1008fs
KIRC	TCGA-B0-5092-01	exon_skip_135112	28847254	28847497	28847383	28847383	Frame_Shift_Del	G	-	p.G1009fs
KIRC	TCGA-B0-5092-01	exon_skip_135112	28847254	28847497	28847383	28847383	Frame_Shift_Del	G	-	p.S1008fs
KIRC	TCGA-B0-5092-01	exon_skip_135114	28847254	28847806	28847383	28847383	Frame_Shift_Del	G	-	p.G1009fs
KIRC	TCGA-B0-5092-01	exon_skip_135114	28847254	28847806	28847383	28847383	Frame_Shift_Del	G	-	p.S1008fs
LIHC	TCGA-G3-A3CJ-01	exon_skip_135114	28847254	28847806	28847515	28847515	Frame_Shift_Del	G	-	p.G1054fs
LIHC	TCGA-G3-A3CJ-01	exon_skip_135114	28847254	28847806	28847675	28847675	Frame_Shift_Del	C	-	p.R1058fs
LIHC	TCGA-G3-A3CJ-01	exon_skip_135139	28847647	28847811	28847675	28847675	Frame_Shift_Del	C	-	p.R1058fs
STAD	TCGA-HU-A4GT-01	exon_skip_135111	28847254	28847443	28847355	28847356	Frame_Shift_Ins	-	C	p.G999fs
STAD	TCGA-HU-A4GT-01	exon_skip_135112	28847254	28847497	28847355	28847356	Frame_Shift_Ins	-	C	p.G999fs
STAD	TCGA-HU-A4GT-01	exon_skip_135114	28847254	28847806	28847355	28847356	Frame_Shift_Ins	-	C	p.G999fs
UCEC	TCGA-B5-A0K0-01	exon_skip_135111	28847254	28847443	28847355	28847356	Frame_Shift_Ins	-	C	p.G999fs
UCEC	TCGA-B5-A0K0-01	exon_skip_135112	28847254	28847497	28847355	28847356	Frame_Shift_Ins	-	C	p.G999fs
UCEC	TCGA-B5-A0K0-01	exon_skip_135114	28847254	28847806	28847355	28847356	Frame_Shift_Ins	-	C	p.G999fs
STAD	TCGA-HU-A4GT-01	exon_skip_135111	28847254	28847443	28847356	28847357	Frame_Shift_Ins	-	C	p.G999fs
STAD	TCGA-HU-A4GT-01	exon_skip_135112	28847254	28847497	28847356	28847357	Frame_Shift_Ins	-	C	p.G999fs
STAD	TCGA-HU-A4GT-01	exon_skip_135114	28847254	28847806	28847356	28847357	Frame_Shift_Ins	-	C	p.G999fs
COAD	TCGA-CA-6717-01	exon_skip_135085	28843817	28843888	28843822	28843822	Nonsense_Mutation	G	T	p.E508X
ESCA	TCGA-2H-A9GG-01A-11D-A37C-09	exon_skip_135100	28844760	28844829	28844774	28844774	Nonsense_Mutation	C	G	p.S657*
LUSC	TCGA-46-3768-01	exon_skip_135111	28847254	28847443	28847341	28847341	Nonsense_Mutation	C	T	p.Q995*
LUSC	TCGA-46-3768-01	exon_skip_135112	28847254	28847497	28847341	28847341	Nonsense_Mutation	C	T	p.Q995*
LUSC	TCGA-46-3768-01	exon_skip_135114	28847254	28847806	28847341	28847341	Nonsense_Mutation	C	T	p.Q995*
KIRC	TCGA-B0-5094-01	exon_skip_135114	28847254	28847806	28847661	28847661	Nonsense_Mutation	A	T	p.R1052*
KIRC	TCGA-B0-5094-01	exon_skip_135114	28847254	28847806	28847661	28847661	Nonsense_Mutation	A	T	p.R1052X
KIRC	TCGA-B0-5094-01	exon_skip_135139	28847647	28847811	28847661	28847661	Nonsense_Mutation	A	T	p.R1052*
KIRC	TCGA-B0-5094-01	exon_skip_135139	28847647	28847811	28847661	28847661	Nonsense_Mutation	A	T	p.R1052X
STAD	TCGA-BR-6452-01	exon_skip_135094	28844138	28844208	28844210	28844210	Splice_Site	T	C	.
STAD	TCGA-BR-6452-01	exon_skip_135094	28844138	28844208	28844210	28844210	Splice_Site	T	C	p.K553_splice

- Depth of coverage in the three exons composing exon skipping event

Depth of coverage in three exons	Mutation description
	Sample: TCGA-B0-5094-01
	Cancer type: KIRC
	ESID: exon_skip_135139
	Skipped exon start: 28847647
	Skipped exon end: 28847811
	Mutation start: 28847661
	Mutation end: 28847661
	Mutation type: Nonsense_Mutation
	Reference seq: A
	Mutation seq: T
	AAchange: p.R1052X
	Sample: TCGA-B0-5094-01
	Cancer type: KIRC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847661
	Mutation end: 28847661
	Mutation type: Nonsense_Mutation
	Reference seq: A
	Mutation seq: T
	AAchange: p.R1052X
	Sample: TCGA-B0-5094-01
	Cancer type: KIRC
	ESID: exon_skip_135139
	Skipped exon start: 28847647
	Skipped exon end: 28847811
	Mutation start: 28847661
	Mutation end: 28847661
	Mutation type: Nonsense_Mutation
	Reference seq: A
	Mutation seq: T
	AAchange: p.R1052*
	Sample: TCGA-B0-5094-01
	Cancer type: KIRC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847661
	Mutation end: 28847661
	Mutation type: Nonsense_Mutation
	Reference seq: A
	Mutation seq: T
	AAchange: p.R1052*
exon_skip_135114_KIRC_TCGA-B0-5094-01.png
exon_skip_384879_KIRC_TCGA-B0-5094-01.png
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
exon_skip_135111_LUSC_TCGA-46-3768-01.png
exon_skip_135112_LUSC_TCGA-46-3768-01.png
exon_skip_135114_LUSC_TCGA-46-3768-01.png
exon_skip_470639_LUSC_TCGA-46-3768-01.png
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135111_COAD_TCGA-AA-3492-01.png
exon_skip_135112_COAD_TCGA-AA-3492-01.png
exon_skip_135114_COAD_TCGA-AA-3492-01.png
exon_skip_73757_COAD_TCGA-AA-3492-01.png
exon_skip_83395_COAD_TCGA-AA-3492-01.png
exon_skip_83396_COAD_TCGA-AA-3492-01.png
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
exon_skip_11218_COAD_TCGA-AZ-6598-01.png
exon_skip_11256_COAD_TCGA-AZ-6598-01.png
exon_skip_11259_COAD_TCGA-AZ-6598-01.png
exon_skip_11263_COAD_TCGA-AZ-6598-01.png
exon_skip_135111_COAD_TCGA-AZ-6598-01.png
exon_skip_135112_COAD_TCGA-AZ-6598-01.png
exon_skip_135114_COAD_TCGA-AZ-6598-01.png
exon_skip_139080_COAD_TCGA-AZ-6598-01.png
exon_skip_142268_COAD_TCGA-AZ-6598-01.png
exon_skip_149455_COAD_TCGA-AZ-6598-01.png
exon_skip_300996_COAD_TCGA-AZ-6598-01.png
exon_skip_303809_COAD_TCGA-AZ-6598-01.png
exon_skip_357723_COAD_TCGA-AZ-6598-01.png
exon_skip_384067_COAD_TCGA-AZ-6598-01.png
exon_skip_384069_COAD_TCGA-AZ-6598-01.png
exon_skip_384070_COAD_TCGA-AZ-6598-01.png
exon_skip_434039_COAD_TCGA-AZ-6598-01.png
exon_skip_434040_COAD_TCGA-AZ-6598-01.png
exon_skip_434375_COAD_TCGA-AZ-6598-01.png
exon_skip_434763_COAD_TCGA-AZ-6598-01.png
exon_skip_439048_COAD_TCGA-AZ-6598-01.png
exon_skip_49506_COAD_TCGA-AZ-6598-01.png
exon_skip_54471_COAD_TCGA-AZ-6598-01.png
exon_skip_54472_COAD_TCGA-AZ-6598-01.png
exon_skip_84515_COAD_TCGA-AZ-6598-01.png
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
exon_skip_108215_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135111_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135112_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135114_HNSC_TCGA-QK-A6VB-01.png
exon_skip_315273_HNSC_TCGA-QK-A6VB-01.png
exon_skip_457890_HNSC_TCGA-QK-A6VB-01.png
exon_skip_81980_HNSC_TCGA-QK-A6VB-01.png
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
exon_skip_135111_KIRC_TCGA-B0-5092-01.png
exon_skip_135112_KIRC_TCGA-B0-5092-01.png
exon_skip_135114_KIRC_TCGA-B0-5092-01.png
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135111_READ_TCGA-EI-6882-01.png
exon_skip_135112_READ_TCGA-EI-6882-01.png
exon_skip_135114_READ_TCGA-EI-6882-01.png
exon_skip_304901_READ_TCGA-EI-6882-01.png
exon_skip_334382_READ_TCGA-EI-6882-01.png
exon_skip_334405_READ_TCGA-EI-6882-01.png
exon_skip_372536_READ_TCGA-EI-6882-01.png
exon_skip_4028_READ_TCGA-EI-6882-01.png
exon_skip_439047_READ_TCGA-EI-6882-01.png
exon_skip_439048_READ_TCGA-EI-6882-01.png
exon_skip_454428_READ_TCGA-EI-6882-01.png
exon_skip_454431_READ_TCGA-EI-6882-01.png
exon_skip_454433_READ_TCGA-EI-6882-01.png
exon_skip_69190_READ_TCGA-EI-6882-01.png
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
exon_skip_121685_STAD_TCGA-HU-A4GT-01.png
exon_skip_135112_STAD_TCGA-HU-A4GT-01.png
exon_skip_135114_STAD_TCGA-HU-A4GT-01.png
exon_skip_295812_STAD_TCGA-HU-A4GT-01.png
exon_skip_310114_STAD_TCGA-HU-A4GT-01.png
exon_skip_314971_STAD_TCGA-HU-A4GT-01.png
exon_skip_328008_STAD_TCGA-HU-A4GT-01.png
exon_skip_347979_STAD_TCGA-HU-A4GT-01.png
exon_skip_347981_STAD_TCGA-HU-A4GT-01.png
exon_skip_45131_STAD_TCGA-HU-A4GT-01.png
exon_skip_45132_STAD_TCGA-HU-A4GT-01.png
exon_skip_65658_STAD_TCGA-HU-A4GT-01.png
exon_skip_86427_STAD_TCGA-HU-A4GT-01.png
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_112411_STAD_TCGA-BR-8372-01.png
exon_skip_135114_STAD_TCGA-BR-8372-01.png
exon_skip_137802_STAD_TCGA-BR-8372-01.png
exon_skip_347779_STAD_TCGA-BR-8372-01.png
exon_skip_347781_STAD_TCGA-BR-8372-01.png
exon_skip_45789_STAD_TCGA-BR-8372-01.png
exon_skip_484840_STAD_TCGA-BR-8372-01.png
exon_skip_5861_STAD_TCGA-BR-8372-01.png
exon_skip_79676_STAD_TCGA-BR-8372-01.png
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135112_STAD_TCGA-BR-6566-01.png
exon_skip_135114_STAD_TCGA-BR-6566-01.png
exon_skip_386802_STAD_TCGA-BR-6566-01.png
exon_skip_478923_STAD_TCGA-BR-6566-01.png
exon_skip_478926_STAD_TCGA-BR-6566-01.png
exon_skip_512765_STAD_TCGA-BR-6566-01.png
exon_skip_512766_STAD_TCGA-BR-6566-01.png
exon_skip_59926_STAD_TCGA-BR-6566-01.png
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-A5-A0GH-01.png
exon_skip_135112_UCEC_TCGA-A5-A0GH-01.png
exon_skip_135114_UCEC_TCGA-A5-A0GH-01.png
exon_skip_137337_UCEC_TCGA-A5-A0GH-01.png
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
exon_skip_135111_UCEC_TCGA-B5-A0K0-01.png
exon_skip_135112_UCEC_TCGA-B5-A0K0-01.png
exon_skip_135114_UCEC_TCGA-B5-A0K0-01.png
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-BG-A0LX-01.png
exon_skip_135112_UCEC_TCGA-BG-A0LX-01.png
exon_skip_135114_UCEC_TCGA-BG-A0LX-01.png
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-D1-A17U-01.png
exon_skip_135112_UCEC_TCGA-D1-A17U-01.png
exon_skip_135114_UCEC_TCGA-D1-A17U-01.png
exon_skip_286384_UCEC_TCGA-D1-A17U-01.png
exon_skip_294586_UCEC_TCGA-D1-A17U-01.png
exon_skip_365789_UCEC_TCGA-D1-A17U-01.png
exon_skip_43714_UCEC_TCGA-D1-A17U-01.png
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
exon_skip_135111_LUSC_TCGA-46-3768-01.png
exon_skip_135112_LUSC_TCGA-46-3768-01.png
exon_skip_135114_LUSC_TCGA-46-3768-01.png
exon_skip_470639_LUSC_TCGA-46-3768-01.png
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135111_COAD_TCGA-AA-3492-01.png
exon_skip_135112_COAD_TCGA-AA-3492-01.png
exon_skip_135114_COAD_TCGA-AA-3492-01.png
exon_skip_73757_COAD_TCGA-AA-3492-01.png
exon_skip_83395_COAD_TCGA-AA-3492-01.png
exon_skip_83396_COAD_TCGA-AA-3492-01.png
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
exon_skip_11218_COAD_TCGA-AZ-6598-01.png
exon_skip_11256_COAD_TCGA-AZ-6598-01.png
exon_skip_11259_COAD_TCGA-AZ-6598-01.png
exon_skip_11263_COAD_TCGA-AZ-6598-01.png
exon_skip_135111_COAD_TCGA-AZ-6598-01.png
exon_skip_135112_COAD_TCGA-AZ-6598-01.png
exon_skip_135114_COAD_TCGA-AZ-6598-01.png
exon_skip_139080_COAD_TCGA-AZ-6598-01.png
exon_skip_142268_COAD_TCGA-AZ-6598-01.png
exon_skip_149455_COAD_TCGA-AZ-6598-01.png
exon_skip_300996_COAD_TCGA-AZ-6598-01.png
exon_skip_303809_COAD_TCGA-AZ-6598-01.png
exon_skip_357723_COAD_TCGA-AZ-6598-01.png
exon_skip_384067_COAD_TCGA-AZ-6598-01.png
exon_skip_384069_COAD_TCGA-AZ-6598-01.png
exon_skip_384070_COAD_TCGA-AZ-6598-01.png
exon_skip_434039_COAD_TCGA-AZ-6598-01.png
exon_skip_434040_COAD_TCGA-AZ-6598-01.png
exon_skip_434375_COAD_TCGA-AZ-6598-01.png
exon_skip_434763_COAD_TCGA-AZ-6598-01.png
exon_skip_439048_COAD_TCGA-AZ-6598-01.png
exon_skip_49506_COAD_TCGA-AZ-6598-01.png
exon_skip_54471_COAD_TCGA-AZ-6598-01.png
exon_skip_54472_COAD_TCGA-AZ-6598-01.png
exon_skip_84515_COAD_TCGA-AZ-6598-01.png
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
exon_skip_108215_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135111_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135112_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135114_HNSC_TCGA-QK-A6VB-01.png
exon_skip_315273_HNSC_TCGA-QK-A6VB-01.png
exon_skip_457890_HNSC_TCGA-QK-A6VB-01.png
exon_skip_81980_HNSC_TCGA-QK-A6VB-01.png
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
exon_skip_135111_KIRC_TCGA-B0-5092-01.png
exon_skip_135112_KIRC_TCGA-B0-5092-01.png
exon_skip_135114_KIRC_TCGA-B0-5092-01.png
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135111_READ_TCGA-EI-6882-01.png
exon_skip_135112_READ_TCGA-EI-6882-01.png
exon_skip_135114_READ_TCGA-EI-6882-01.png
exon_skip_304901_READ_TCGA-EI-6882-01.png
exon_skip_334382_READ_TCGA-EI-6882-01.png
exon_skip_334405_READ_TCGA-EI-6882-01.png
exon_skip_372536_READ_TCGA-EI-6882-01.png
exon_skip_4028_READ_TCGA-EI-6882-01.png
exon_skip_439047_READ_TCGA-EI-6882-01.png
exon_skip_439048_READ_TCGA-EI-6882-01.png
exon_skip_454428_READ_TCGA-EI-6882-01.png
exon_skip_454431_READ_TCGA-EI-6882-01.png
exon_skip_454433_READ_TCGA-EI-6882-01.png
exon_skip_69190_READ_TCGA-EI-6882-01.png
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
exon_skip_121685_STAD_TCGA-HU-A4GT-01.png
exon_skip_135112_STAD_TCGA-HU-A4GT-01.png
exon_skip_135114_STAD_TCGA-HU-A4GT-01.png
exon_skip_295812_STAD_TCGA-HU-A4GT-01.png
exon_skip_310114_STAD_TCGA-HU-A4GT-01.png
exon_skip_314971_STAD_TCGA-HU-A4GT-01.png
exon_skip_328008_STAD_TCGA-HU-A4GT-01.png
exon_skip_347979_STAD_TCGA-HU-A4GT-01.png
exon_skip_347981_STAD_TCGA-HU-A4GT-01.png
exon_skip_45131_STAD_TCGA-HU-A4GT-01.png
exon_skip_45132_STAD_TCGA-HU-A4GT-01.png
exon_skip_65658_STAD_TCGA-HU-A4GT-01.png
exon_skip_86427_STAD_TCGA-HU-A4GT-01.png
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_112411_STAD_TCGA-BR-8372-01.png
exon_skip_135114_STAD_TCGA-BR-8372-01.png
exon_skip_137802_STAD_TCGA-BR-8372-01.png
exon_skip_347779_STAD_TCGA-BR-8372-01.png
exon_skip_347781_STAD_TCGA-BR-8372-01.png
exon_skip_45789_STAD_TCGA-BR-8372-01.png
exon_skip_484840_STAD_TCGA-BR-8372-01.png
exon_skip_5861_STAD_TCGA-BR-8372-01.png
exon_skip_79676_STAD_TCGA-BR-8372-01.png
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135112_STAD_TCGA-BR-6566-01.png
exon_skip_135114_STAD_TCGA-BR-6566-01.png
exon_skip_386802_STAD_TCGA-BR-6566-01.png
exon_skip_478923_STAD_TCGA-BR-6566-01.png
exon_skip_478926_STAD_TCGA-BR-6566-01.png
exon_skip_512765_STAD_TCGA-BR-6566-01.png
exon_skip_512766_STAD_TCGA-BR-6566-01.png
exon_skip_59926_STAD_TCGA-BR-6566-01.png
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-A5-A0GH-01.png
exon_skip_135112_UCEC_TCGA-A5-A0GH-01.png
exon_skip_135114_UCEC_TCGA-A5-A0GH-01.png
exon_skip_137337_UCEC_TCGA-A5-A0GH-01.png
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
exon_skip_135111_UCEC_TCGA-B5-A0K0-01.png
exon_skip_135112_UCEC_TCGA-B5-A0K0-01.png
exon_skip_135114_UCEC_TCGA-B5-A0K0-01.png
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-BG-A0LX-01.png
exon_skip_135112_UCEC_TCGA-BG-A0LX-01.png
exon_skip_135114_UCEC_TCGA-BG-A0LX-01.png
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-D1-A17U-01.png
exon_skip_135112_UCEC_TCGA-D1-A17U-01.png
exon_skip_135114_UCEC_TCGA-D1-A17U-01.png
exon_skip_286384_UCEC_TCGA-D1-A17U-01.png
exon_skip_294586_UCEC_TCGA-D1-A17U-01.png
exon_skip_365789_UCEC_TCGA-D1-A17U-01.png
exon_skip_43714_UCEC_TCGA-D1-A17U-01.png
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
	Sample: TCGA-46-3768-01
	Cancer type: LUSC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847341
	Mutation end: 28847341
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q995*
exon_skip_135111_LUSC_TCGA-46-3768-01.png
exon_skip_135112_LUSC_TCGA-46-3768-01.png
exon_skip_135114_LUSC_TCGA-46-3768-01.png
exon_skip_470639_LUSC_TCGA-46-3768-01.png
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-AA-3492-01
	Cancer type: COAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135111_COAD_TCGA-AA-3492-01.png
exon_skip_135112_COAD_TCGA-AA-3492-01.png
exon_skip_135114_COAD_TCGA-AA-3492-01.png
exon_skip_73757_COAD_TCGA-AA-3492-01.png
exon_skip_83395_COAD_TCGA-AA-3492-01.png
exon_skip_83396_COAD_TCGA-AA-3492-01.png
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-AZ-6598-01
	Cancer type: COAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
exon_skip_11218_COAD_TCGA-AZ-6598-01.png
exon_skip_11256_COAD_TCGA-AZ-6598-01.png
exon_skip_11259_COAD_TCGA-AZ-6598-01.png
exon_skip_11263_COAD_TCGA-AZ-6598-01.png
exon_skip_135111_COAD_TCGA-AZ-6598-01.png
exon_skip_135112_COAD_TCGA-AZ-6598-01.png
exon_skip_135114_COAD_TCGA-AZ-6598-01.png
exon_skip_139080_COAD_TCGA-AZ-6598-01.png
exon_skip_142268_COAD_TCGA-AZ-6598-01.png
exon_skip_149455_COAD_TCGA-AZ-6598-01.png
exon_skip_300996_COAD_TCGA-AZ-6598-01.png
exon_skip_303809_COAD_TCGA-AZ-6598-01.png
exon_skip_357723_COAD_TCGA-AZ-6598-01.png
exon_skip_384067_COAD_TCGA-AZ-6598-01.png
exon_skip_384069_COAD_TCGA-AZ-6598-01.png
exon_skip_384070_COAD_TCGA-AZ-6598-01.png
exon_skip_434039_COAD_TCGA-AZ-6598-01.png
exon_skip_434040_COAD_TCGA-AZ-6598-01.png
exon_skip_434375_COAD_TCGA-AZ-6598-01.png
exon_skip_434763_COAD_TCGA-AZ-6598-01.png
exon_skip_439048_COAD_TCGA-AZ-6598-01.png
exon_skip_49506_COAD_TCGA-AZ-6598-01.png
exon_skip_54471_COAD_TCGA-AZ-6598-01.png
exon_skip_54472_COAD_TCGA-AZ-6598-01.png
exon_skip_84515_COAD_TCGA-AZ-6598-01.png
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-QK-A6VB-01
	Cancer type: HNSC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G999fs
exon_skip_108215_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135111_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135112_HNSC_TCGA-QK-A6VB-01.png
exon_skip_135114_HNSC_TCGA-QK-A6VB-01.png
exon_skip_315273_HNSC_TCGA-QK-A6VB-01.png
exon_skip_457890_HNSC_TCGA-QK-A6VB-01.png
exon_skip_81980_HNSC_TCGA-QK-A6VB-01.png
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.S1008fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
	Sample: TCGA-B0-5092-01
	Cancer type: KIRC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847383
	Mutation end: 28847383
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G1009fs
exon_skip_135111_KIRC_TCGA-B0-5092-01.png
exon_skip_135112_KIRC_TCGA-B0-5092-01.png
exon_skip_135114_KIRC_TCGA-B0-5092-01.png
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-EI-6882-01
	Cancer type: READ
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135111_READ_TCGA-EI-6882-01.png
exon_skip_135112_READ_TCGA-EI-6882-01.png
exon_skip_135114_READ_TCGA-EI-6882-01.png
exon_skip_304901_READ_TCGA-EI-6882-01.png
exon_skip_334382_READ_TCGA-EI-6882-01.png
exon_skip_334405_READ_TCGA-EI-6882-01.png
exon_skip_372536_READ_TCGA-EI-6882-01.png
exon_skip_4028_READ_TCGA-EI-6882-01.png
exon_skip_439047_READ_TCGA-EI-6882-01.png
exon_skip_439048_READ_TCGA-EI-6882-01.png
exon_skip_454428_READ_TCGA-EI-6882-01.png
exon_skip_454431_READ_TCGA-EI-6882-01.png
exon_skip_454433_READ_TCGA-EI-6882-01.png
exon_skip_69190_READ_TCGA-EI-6882-01.png
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-HU-A4GT-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847357
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
exon_skip_121685_STAD_TCGA-HU-A4GT-01.png
exon_skip_135112_STAD_TCGA-HU-A4GT-01.png
exon_skip_135114_STAD_TCGA-HU-A4GT-01.png
exon_skip_295812_STAD_TCGA-HU-A4GT-01.png
exon_skip_310114_STAD_TCGA-HU-A4GT-01.png
exon_skip_314971_STAD_TCGA-HU-A4GT-01.png
exon_skip_328008_STAD_TCGA-HU-A4GT-01.png
exon_skip_347979_STAD_TCGA-HU-A4GT-01.png
exon_skip_347981_STAD_TCGA-HU-A4GT-01.png
exon_skip_45131_STAD_TCGA-HU-A4GT-01.png
exon_skip_45132_STAD_TCGA-HU-A4GT-01.png
exon_skip_65658_STAD_TCGA-HU-A4GT-01.png
exon_skip_86427_STAD_TCGA-HU-A4GT-01.png
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847356
	Mutation end: 28847356
	Mutation type: Frame_Shift_Del
	Reference seq: C
	Mutation seq: -
	AAchange: p.G999fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-8372-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_112411_STAD_TCGA-BR-8372-01.png
exon_skip_135114_STAD_TCGA-BR-8372-01.png
exon_skip_137802_STAD_TCGA-BR-8372-01.png
exon_skip_347779_STAD_TCGA-BR-8372-01.png
exon_skip_347781_STAD_TCGA-BR-8372-01.png
exon_skip_45789_STAD_TCGA-BR-8372-01.png
exon_skip_484840_STAD_TCGA-BR-8372-01.png
exon_skip_5861_STAD_TCGA-BR-8372-01.png
exon_skip_79676_STAD_TCGA-BR-8372-01.png
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
	Sample: TCGA-BR-6566-01
	Cancer type: STAD
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.H997fs
exon_skip_135112_STAD_TCGA-BR-6566-01.png
exon_skip_135114_STAD_TCGA-BR-6566-01.png
exon_skip_386802_STAD_TCGA-BR-6566-01.png
exon_skip_478923_STAD_TCGA-BR-6566-01.png
exon_skip_478926_STAD_TCGA-BR-6566-01.png
exon_skip_512765_STAD_TCGA-BR-6566-01.png
exon_skip_512766_STAD_TCGA-BR-6566-01.png
exon_skip_59926_STAD_TCGA-BR-6566-01.png
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-A5-A0GH-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-A5-A0GH-01.png
exon_skip_135112_UCEC_TCGA-A5-A0GH-01.png
exon_skip_135114_UCEC_TCGA-A5-A0GH-01.png
exon_skip_137337_UCEC_TCGA-A5-A0GH-01.png
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
	Sample: TCGA-B5-A0K0-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847355
	Mutation end: 28847356
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: C
	AAchange: p.G999fs
exon_skip_135111_UCEC_TCGA-B5-A0K0-01.png
exon_skip_135112_UCEC_TCGA-B5-A0K0-01.png
exon_skip_135114_UCEC_TCGA-B5-A0K0-01.png
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-BG-A0LX-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-BG-A0LX-01.png
exon_skip_135112_UCEC_TCGA-BG-A0LX-01.png
exon_skip_135114_UCEC_TCGA-BG-A0LX-01.png
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135111
	Skipped exon start: 28847254
	Skipped exon end: 28847443
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135112
	Skipped exon start: 28847254
	Skipped exon end: 28847497
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
	Sample: TCGA-D1-A17U-01
	Cancer type: UCEC
	ESID: exon_skip_135114
	Skipped exon start: 28847254
	Skipped exon end: 28847806
	Mutation start: 28847350
	Mutation end: 28847350
	Mutation type: Frame_Shift_Del
	Reference seq: G
	Mutation seq: -
	AAchange: p.G998fs
exon_skip_135111_UCEC_TCGA-D1-A17U-01.png
exon_skip_135112_UCEC_TCGA-D1-A17U-01.png
exon_skip_135114_UCEC_TCGA-D1-A17U-01.png
exon_skip_286384_UCEC_TCGA-D1-A17U-01.png
exon_skip_294586_UCEC_TCGA-D1-A17U-01.png
exon_skip_365789_UCEC_TCGA-D1-A17U-01.png
exon_skip_43714_UCEC_TCGA-D1-A17U-01.png
	Sample: TCGA-CA-6717-01
	Cancer type: COAD
	ESID: exon_skip_135085
	Skipped exon start: 28843817
	Skipped exon end: 28843888
	Mutation start: 28843822
	Mutation end: 28843822
	Mutation type: Nonsense_Mutation
	Reference seq: G
	Mutation seq: T
	AAchange: p.E508X
exon_skip_107202_COAD_TCGA-CA-6717-01.png
exon_skip_135085_COAD_TCGA-CA-6717-01.png
exon_skip_284772_COAD_TCGA-CA-6717-01.png
exon_skip_28826_COAD_TCGA-CA-6717-01.png
exon_skip_304901_COAD_TCGA-CA-6717-01.png
exon_skip_430052_COAD_TCGA-CA-6717-01.png
exon_skip_430053_COAD_TCGA-CA-6717-01.png
exon_skip_433462_COAD_TCGA-CA-6717-01.png
exon_skip_439050_COAD_TCGA-CA-6717-01.png
exon_skip_482455_COAD_TCGA-CA-6717-01.png
exon_skip_503414_COAD_TCGA-CA-6717-01.png

- Non-synonymous mutations located in the skipped exons in CCLE.

Sample	Skipped exon start	Skipped exon end	Mutation start	Mutation end	Mutation type	Reference seq	Mutation seq	AAchange
CMLT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28838183	28838307	28838262	28838262	Frame_Shift_Del	G	-	p.E232fs
HEC151_ENDOMETRIUM	28838183	28838307	28838262	28838262	Frame_Shift_Del	G	-	p.E232fs
HEC265_ENDOMETRIUM	28838183	28838307	28838262	28838262	Frame_Shift_Del	G	-	p.E232fs
SNU1_STOMACH	28838183	28838307	28838262	28838262	Frame_Shift_Del	G	-	p.E232fs
JHUEM1_ENDOMETRIUM	28838183	28838307	28838262	28838262	Frame_Shift_Del	G	-	p.E232fs
DOV13_OVARY	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
DOV13_OVARY	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
DOV13_OVARY	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
HEC59_ENDOMETRIUM	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
HEC59_ENDOMETRIUM	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
HEC59_ENDOMETRIUM	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
2313287_STOMACH	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
2313287_STOMACH	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
2313287_STOMACH	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
EFO27_OVARY	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
EFO27_OVARY	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
EFO27_OVARY	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
HCT116_LARGE_INTESTINE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
HCT116_LARGE_INTESTINE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
HCT116_LARGE_INTESTINE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
SNU1_STOMACH	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
SNU1_STOMACH	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
SNU1_STOMACH	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
GP2D_LARGE_INTESTINE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
GP2D_LARGE_INTESTINE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
GP2D_LARGE_INTESTINE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
RL952_ENDOMETRIUM	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
RL952_ENDOMETRIUM	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
RL952_ENDOMETRIUM	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
639V_URINARY_TRACT	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
639V_URINARY_TRACT	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
639V_URINARY_TRACT	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
CW2_LARGE_INTESTINE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
CW2_LARGE_INTESTINE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
CW2_LARGE_INTESTINE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
GP5D_LARGE_INTESTINE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
GP5D_LARGE_INTESTINE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
GP5D_LARGE_INTESTINE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
LIM1215_LARGE_INTESTINE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
LIM1215_LARGE_INTESTINE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
LIM1215_LARGE_INTESTINE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
SNUC5_LARGE_INTESTINE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
SNUC5_LARGE_INTESTINE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
SNUC5_LARGE_INTESTINE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
WSUNHL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
WSUNHL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
WSUNHL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847350	28847350	Frame_Shift_Del	G	-	p.G999fs
MCC26_SKIN	28842283	28842393	28842289	28842289	Missense_Mutation	C	T	p.S406F
SNU1040_LARGE_INTESTINE	28842283	28842393	28842291	28842291	Missense_Mutation	C	T	p.R407C
NCIH23_LUNG	28842306	28842393	28842349	28842349	Missense_Mutation	G	T	p.S426I
NCIH23_LUNG	28842283	28842393	28842349	28842349	Missense_Mutation	G	T	p.S426I
TUR_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28842306	28842393	28842355	28842355	Missense_Mutation	G	A	p.R428K
TUR_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28842283	28842393	28842355	28842355	Missense_Mutation	G	A	p.R428K
U937_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28842306	28842393	28842355	28842355	Missense_Mutation	G	A	p.R428K
U937_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28842283	28842393	28842355	28842355	Missense_Mutation	G	A	p.R428K
KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28842306	28842393	28842390	28842390	Missense_Mutation	G	A	p.A440T
KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28842283	28842393	28842390	28842390	Missense_Mutation	G	A	p.A440T
HT55_LARGE_INTESTINE	28844138	28844208	28844189	28844189	Missense_Mutation	A	C	p.K547T
ML1_THYROID	28844138	28844208	28844189	28844189	Missense_Mutation	A	C	p.K547T
HEC108_ENDOMETRIUM	28844760	28844829	28844807	28844807	Missense_Mutation	C	A	p.P668H
CCK81_LARGE_INTESTINE	28846599	28846720	28846604	28846604	Missense_Mutation	G	A	p.V857I
ROS50_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28846599	28846720	28846607	28846607	Missense_Mutation	C	A	p.H858N
MEWO_SKIN	28846599	28846720	28846614	28846615	Missense_Mutation	CC	TT	p.S860F
MEWO_SKIN	28846599	28846720	28846614	28846614	Missense_Mutation	C	T	p.S860F
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847272	28847272	Missense_Mutation	A	G	p.I972V
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847272	28847272	Missense_Mutation	A	G	p.I972V
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847272	28847272	Missense_Mutation	A	G	p.I972V
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847344	28847344	Missense_Mutation	A	G	p.S996G
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847344	28847344	Missense_Mutation	A	G	p.S996G
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847344	28847344	Missense_Mutation	A	G	p.S996G
BICR18_UPPER_AERODIGESTIVE_TRACT	28847254	28847443	28847344	28847344	Missense_Mutation	A	G	p.S996G
BICR18_UPPER_AERODIGESTIVE_TRACT	28847254	28847497	28847344	28847344	Missense_Mutation	A	G	p.S996G
BICR18_UPPER_AERODIGESTIVE_TRACT	28847254	28847806	28847344	28847344	Missense_Mutation	A	G	p.S996G
BICR18_UPPER_AERODIGESTIVE_TRACT	28847254	28847443	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
BICR18_UPPER_AERODIGESTIVE_TRACT	28847254	28847497	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
BICR18_UPPER_AERODIGESTIVE_TRACT	28847254	28847806	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
OCIAML5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
OCIAML5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
OCIAML5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847378	28847378	Missense_Mutation	A	C	p.Q1007P
LAMA84_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847389	28847389	Missense_Mutation	C	A	p.P1011T
LAMA84_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847389	28847389	Missense_Mutation	C	A	p.P1011T
LAMA84_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847389	28847389	Missense_Mutation	C	A	p.P1011T
MOLM13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847443	28847410	28847410	Missense_Mutation	C	G	p.P1018A
MOLM13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847497	28847410	28847410	Missense_Mutation	C	G	p.P1018A
MOLM13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847410	28847410	Missense_Mutation	C	G	p.P1018A
BECKER_CENTRAL_NERVOUS_SYSTEM	28847254	28847443	28847410	28847410	Missense_Mutation	C	A	p.P1018T
BECKER_CENTRAL_NERVOUS_SYSTEM	28847254	28847497	28847410	28847410	Missense_Mutation	C	A	p.P1018T
BECKER_CENTRAL_NERVOUS_SYSTEM	28847254	28847806	28847410	28847410	Missense_Mutation	C	A	p.P1018T
SNUC2A_LARGE_INTESTINE	28847254	28847443	28847437	28847437	Missense_Mutation	C	T	p.P1027S
SNUC2A_LARGE_INTESTINE	28847254	28847497	28847437	28847437	Missense_Mutation	C	T	p.P1027S
SNUC2A_LARGE_INTESTINE	28847254	28847806	28847437	28847437	Missense_Mutation	C	T	p.P1027S
LNCAPCLONEFGC_PROSTATE	28847254	28847497	28847456	28847456	Missense_Mutation	G	A	p.G1033D
LNCAPCLONEFGC_PROSTATE	28847254	28847806	28847456	28847456	Missense_Mutation	G	A	p.G1033D
KYSE50_OESOPHAGUS	28847254	28847497	28847458	28847458	Missense_Mutation	C	A	p.Q1034K
KYSE50_OESOPHAGUS	28847254	28847806	28847458	28847458	Missense_Mutation	C	A	p.Q1034K
HEC251_ENDOMETRIUM	28847254	28847497	28847485	28847485	Missense_Mutation	G	A	p.D1043N
HEC251_ENDOMETRIUM	28847254	28847806	28847485	28847485	Missense_Mutation	G	A	p.D1043N
HT115_LARGE_INTESTINE	28847254	28847497	28847488	28847488	Missense_Mutation	G	T	p.D1044Y
HT115_LARGE_INTESTINE	28847254	28847806	28847488	28847488	Missense_Mutation	G	T	p.D1044Y
CTV1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847559	28847559	Missense_Mutation	G	T	p.Q1067H
CCK81_LARGE_INTESTINE	28847254	28847806	28847566	28847566	Missense_Mutation	C	T	p.R1070W
NCIH630_LARGE_INTESTINE	28847254	28847806	28847566	28847566	Missense_Mutation	C	T	p.R1070W
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847583	28847583	Missense_Mutation	G	T	p.E1075D
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847583	28847583	Missense_Mutation	G	T	p.E1075D
OCIAML5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	28847254	28847806	28847583	28847583	Missense_Mutation	G	T	p.E1075D
BICR18_UPPER_AERODIGESTIVE_TRACT	28847254	28847806	28847583	28847583	Missense_Mutation	G	T	p.E1075D
MFE319_ENDOMETRIUM	28844138	28844208	28844208	28844208	Splice_Site	G	A	p.K553K

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ATXN2L

sQTL information located at the skipped exons.

Exon skip ID

Chromosome

Three exons

Skippped exon

ENST

Cancer type

SNP id

Location

DNA change (ref/var)

P-value

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ATXN2L

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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ATXN2L

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RelatedDrugs for ATXN2L

Approved drugs targeting this gene. (DrugBank Version 5.1.0 2018-04-02)

Gene

UniProtAcc

DrugBank ID

Drug name

Drug activity

Drug type

Drug status

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RelatedDiseases for ATXN2L

Diseases associated with this gene. (DisGeNet 4.0)

Gene

Disease ID

Disease name

# pubmeds

Source

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