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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 ZNF638

Gene summary

Gene information	Gene symbol	ZNF638
	Gene ID	27332
	Gene name	zinc finger protein 638
	Synonyms	NP220|ZFML|Zfp638
	Cytomap	2p13.3-p13.2
	Type of gene	protein-coding
	Description	zinc finger protein 638CTCL tumor antigen se33-1CTCL-associated antigen se33-1NP220 nuclear proteincutaneous T-cell lymphoma-associated antigen se33-1nuclear protein 220zinc finger matrin-like protein
	Modification date	20180519
	UniProtAcc	Q14966
	Context	PubMed: ZNF638 [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

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Exon skipping events across known transcript of Ensembl for ZNF638 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 ZNF638

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 ZNF638

Information of exkip skipping event in TCGA.

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_326401	2	71503774:71503884:71575882:71577401:71582848:71582898	71575882:71577401	ENSG00000075292.14	ENST00000410075.1
exon_skip_326404	2	71558911:71558995:71561630:71561726:71575882:71576172	71561630:71561726	ENSG00000075292.14	ENST00000455226.1
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENSG00000075292.14	ENST00000409544.1
exon_skip_326409	2	71558911:71559005:71561630:71561726:71575882:71576172	71561630:71561726	ENSG00000075292.14	ENST00000454278.1
exon_skip_326412	2	71558911:71559005:71575882:71577401:71582848:71582910	71575882:71577401	ENSG00000075292.14	ENST00000377802.2,ENST00000264447.4,ENST00000355812.3
exon_skip_326416	2	71582848:71582910:71588774:71588825:71590282:71590321	71588774:71588825	ENSG00000075292.14	ENST00000466330.1
exon_skip_326419	2	71590282:71590321:71591083:71591382:71592558:71592618	71591083:71591382	ENSG00000075292.14	ENST00000494621.1,ENST00000466975.1,ENST00000377802.2,ENST00000410075.1,ENST00000409544.1,ENST00000475743.1,ENST00000264447.4,ENST00000355812.3,ENST00000464375.1,ENST00000466330.1
exon_skip_326422	2	71592558:71592836:71595511:71595658:71597012:71597135	71595511:71595658	ENSG00000075292.14	ENST00000377802.2,ENST00000410075.1,ENST00000409544.1,ENST00000601581.1,ENST00000264447.4,ENST00000355812.3
exon_skip_326427	2	71607645:71607695:71607967:71608033:71623270:71623321	71607967:71608033	ENSG00000075292.14	ENST00000491843.1
exon_skip_326428	2	71607645:71607695:71615752:71615853:71620523:71620775	71615752:71615853	ENSG00000075292.14	ENST00000410075.1
exon_skip_326429	2	71607642:71607695:71623270:71623321:71625830:71625887	71623270:71623321	ENSG00000075292.14	ENST00000409544.1,ENST00000264447.4,ENST00000355812.3
exon_skip_326430	2	71633257:71633392:71635251:71635377:71645731:71645769	71635251:71635377	ENSG00000075292.14	ENST00000409544.1,ENST00000264447.4,ENST00000487638.1,ENST00000355812.3,ENST00000494241.1
exon_skip_326432	2	71645731:71645769:71649943:71651168:71651779:71651845	71649943:71651168	ENSG00000075292.14	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENSG00000075292.14	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3
exon_skip_326446	2	71654479:71654544:71655660:71655781:71658456:71658558	71655660:71655781	ENSG00000075292.14	ENST00000472758.1
exon_skip_326448	2	71654479:71654544:71655676:71655781:71658456:71658558	71655676:71655781	ENSG00000075292.14	ENST00000409544.1,ENST00000461991.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3
exon_skip_326451	2	71654479:71654544:71658456:71658558:71660294:71660413	71658456:71658558	ENSG00000075292.14	ENST00000493576.2
exon_skip_326455	2	71660294:71660413:71660605:71660665:71661871:71661933	71660605:71660665	ENSG00000075292.14	ENST00000461991.1

PSI values of skipped exons in TCGA.

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Exon skipping events with PSIs in GTEx for ZNF638

Information of exkip skipping event in GTEx

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_326401	2	71503774:71503884:71575882:71577401:71582848:71582898	71575882:71577401	ENSG00000075292.14	ENST00000410075.1
exon_skip_326404	2	71558911:71558995:71561630:71561726:71575882:71576172	71561630:71561726	ENSG00000075292.14	ENST00000455226.1
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENSG00000075292.14	ENST00000409544.1
exon_skip_326409	2	71558911:71559005:71561630:71561726:71575882:71576172	71561630:71561726	ENSG00000075292.14	ENST00000454278.1
exon_skip_326412	2	71558911:71559005:71575882:71577401:71582848:71582910	71575882:71577401	ENSG00000075292.14	ENST00000355812.3,ENST00000377802.2,ENST00000264447.4
exon_skip_326416	2	71582848:71582910:71588774:71588825:71590282:71590321	71588774:71588825	ENSG00000075292.14	ENST00000466330.1
exon_skip_326419	2	71590282:71590321:71591083:71591382:71592558:71592618	71591083:71591382	ENSG00000075292.14	ENST00000494621.1,ENST00000466975.1,ENST00000410075.1,ENST00000466330.1,ENST00000355812.3,ENST00000377802.2,ENST00000464375.1,ENST00000475743.1,ENST00000264447.4,ENST00000409544.1
exon_skip_326422	2	71592558:71592836:71595511:71595658:71597012:71597135	71595511:71595658	ENSG00000075292.14	ENST00000410075.1,ENST00000355812.3,ENST00000377802.2,ENST00000264447.4,ENST00000409544.1,ENST00000601581.1
exon_skip_326427	2	71607645:71607695:71607967:71608033:71623270:71623321	71607967:71608033	ENSG00000075292.14	ENST00000491843.1
exon_skip_326428	2	71607645:71607695:71615752:71615853:71620523:71620775	71615752:71615853	ENSG00000075292.14	ENST00000410075.1
exon_skip_326429	2	71607642:71607695:71623270:71623321:71625830:71625887	71623270:71623321	ENSG00000075292.14	ENST00000355812.3,ENST00000264447.4,ENST00000409544.1
exon_skip_326430	2	71633257:71633392:71635251:71635377:71645731:71645769	71635251:71635377	ENSG00000075292.14	ENST00000355812.3,ENST00000264447.4,ENST00000409544.1,ENST00000487638.1,ENST00000494241.1
exon_skip_326432	2	71645731:71645769:71649943:71651168:71651779:71651845	71649943:71651168	ENSG00000075292.14	ENST00000264447.4,ENST00000409544.1,ENST00000487638.1,ENST00000409407.1
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENSG00000075292.14	ENST00000355812.3,ENST00000264447.4,ENST00000409544.1,ENST00000487638.1,ENST00000409407.1,ENST00000483421.3
exon_skip_326446	2	71654479:71654544:71655660:71655781:71658456:71658558	71655660:71655781	ENSG00000075292.14	ENST00000472758.1
exon_skip_326448	2	71654479:71654544:71655676:71655781:71658456:71658558	71655676:71655781	ENSG00000075292.14	ENST00000355812.3,ENST00000264447.4,ENST00000409544.1,ENST00000487638.1,ENST00000409407.1,ENST00000483421.3,ENST00000461991.1
exon_skip_326451	2	71654479:71654544:71658456:71658558:71660294:71660413	71658456:71658558	ENSG00000075292.14	ENST00000493576.2
exon_skip_326455	2	71660294:71660413:71660605:71660665:71661871:71661933	71660605:71660665	ENSG00000075292.14	ENST00000461991.1

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 ZNF638

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
ENST00000409544	71575556	71577401	5CDS-5UTR
ENST00000264447	71575882	71577401	5CDS-5UTR
ENST00000264447	71591083	71591382	Frame-shift
ENST00000409544	71591083	71591382	Frame-shift
ENST00000264447	71649943	71651168	Frame-shift
ENST00000409544	71649943	71651168	Frame-shift
ENST00000264447	71653589	71654544	Frame-shift
ENST00000409544	71653589	71654544	Frame-shift
ENST00000264447	71595511	71595658	In-frame
ENST00000409544	71595511	71595658	In-frame
ENST00000264447	71623270	71623321	In-frame
ENST00000409544	71623270	71623321	In-frame
ENST00000264447	71635251	71635377	In-frame
ENST00000409544	71635251	71635377	In-frame
ENST00000264447	71655676	71655781	In-frame
ENST00000409544	71655676	71655781	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
ENST00000409544	71575556	71577401	5CDS-5UTR
ENST00000264447	71575882	71577401	5CDS-5UTR
ENST00000264447	71591083	71591382	Frame-shift
ENST00000409544	71591083	71591382	Frame-shift
ENST00000264447	71649943	71651168	Frame-shift
ENST00000409544	71649943	71651168	Frame-shift
ENST00000264447	71653589	71654544	Frame-shift
ENST00000409544	71653589	71654544	Frame-shift
ENST00000264447	71595511	71595658	In-frame
ENST00000409544	71595511	71595658	In-frame
ENST00000264447	71623270	71623321	In-frame
ENST00000409544	71623270	71623321	In-frame
ENST00000264447	71635251	71635377	In-frame
ENST00000409544	71635251	71635377	In-frame
ENST00000264447	71655676	71655781	In-frame
ENST00000409544	71655676	71655781	In-frame

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Infer the effects of exon skipping event on protein functional features for ZNF638

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
ENST00000264447	6522	1978	71595511	71595658	2310	2456	665	714
ENST00000409544	6838	1978	71595511	71595658	2626	2772	665	714
ENST00000264447	6522	1978	71623270	71623321	2692	2742	792	809
ENST00000409544	6838	1978	71623270	71623321	3008	3058	792	809
ENST00000264447	6522	1978	71635251	71635377	3450	3575	1045	1087
ENST00000409544	6838	1978	71635251	71635377	3766	3891	1045	1087
ENST00000264447	6522	1978	71655676	71655781	5860	5964	1848	1883
ENST00000409544	6838	1978	71655676	71655781	6176	6280	1848	1883

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
ENST00000264447	6522	1978	71595511	71595658	2310	2456	665	714
ENST00000409544	6838	1978	71595511	71595658	2626	2772	665	714
ENST00000264447	6522	1978	71623270	71623321	2692	2742	792	809
ENST00000409544	6838	1978	71623270	71623321	3008	3058	792	809
ENST00000264447	6522	1978	71635251	71635377	3450	3575	1045	1087
ENST00000409544	6838	1978	71635251	71635377	3766	3891	1045	1087
ENST00000264447	6522	1978	71655676	71655781	5860	5964	1848	1883
ENST00000409544	6838	1978	71655676	71655781	6176	6280	1848	1883

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 ZNF638

- 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.

ZNF638_HNSC_exon_skip_326432_psi_boxplot.png

ZNF638_HNSC_exon_skip_326437_psi_boxplot.png

ZNF638_LIHC_exon_skip_326432_psi_boxplot.png

ZNF638_LIHC_exon_skip_326437_psi_boxplot.png

ZNF638_LIHC_exon_skip_326448_psi_boxplot.png

ZNF638_LUAD_exon_skip_326432_psi_boxplot.png

ZNF638_LUAD_exon_skip_326437_psi_boxplot.png

ZNF638_STAD_exon_skip_326432_psi_boxplot.png

ZNF638_STAD_exon_skip_326437_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
COAD	TCGA-A6-5665-01	exon_skip_326406	71575557	71577401	71576670	71576673	Frame_Shift_Del	AAAG	-	p.195_196del
COAD	TCGA-A6-5665-01	exon_skip_326401 exon_skip_326412	71575883	71577401	71576670	71576673	Frame_Shift_Del	AAAG	-	p.195_196del
LIHC	TCGA-DD-AADC-01	exon_skip_326406	71575557	71577401	71576746	71576746	Frame_Shift_Del	A	-	p.E221fs
LIHC	TCGA-DD-AADC-01	exon_skip_326401 exon_skip_326412	71575883	71577401	71576746	71576746	Frame_Shift_Del	A	-	p.E221fs
LIHC	TCGA-DD-A3A0-01	exon_skip_326406	71575557	71577401	71576849	71576849	Frame_Shift_Del	A	-	p.P255fs
LIHC	TCGA-DD-A3A0-01	exon_skip_326401 exon_skip_326412	71575883	71577401	71576849	71576849	Frame_Shift_Del	A	-	p.P255fs
LIHC	TCGA-DD-A39Y-01	exon_skip_326406	71575557	71577401	71577092	71577092	Frame_Shift_Del	T	-	p.P336fs
LIHC	TCGA-DD-A39Y-01	exon_skip_326401 exon_skip_326412	71575883	71577401	71577092	71577092	Frame_Shift_Del	T	-	p.P336fs
LIHC	TCGA-G3-A3CJ-01	exon_skip_326419	71591084	71591382	71591281	71591281	Frame_Shift_Del	C	-	p.S539fs
LIHC	TCGA-DD-A3A0-01	exon_skip_326419	71591084	71591382	71591299	71591299	Frame_Shift_Del	T	-	p.I545fs
STAD	TCGA-BR-4201-01	exon_skip_326432	71649944	71651168	71649954	71649954	Frame_Shift_Del	A	-	p.L1103fs
LIHC	TCGA-DD-A3A0-01	exon_skip_326432	71649944	71651168	71650512	71650512	Frame_Shift_Del	G	-	p.G1290fs
LIHC	TCGA-G3-A3CJ-01	exon_skip_326432	71649944	71651168	71650512	71650512	Frame_Shift_Del	G	-	p.G1290fs
LIHC	TCGA-DD-A39Y-01	exon_skip_326432	71649944	71651168	71650533	71650533	Frame_Shift_Del	A	-	p.K1298fs
HNSC	TCGA-F7-A624-01	exon_skip_326432	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
LIHC	TCGA-DD-A1EG-01	exon_skip_326432	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
LUAD	TCGA-86-A4JF-01	exon_skip_326432	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
UCEC	TCGA-A5-A0G9-01	exon_skip_326432	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
LIHC	TCGA-G3-A3CJ-01	exon_skip_326432	71649944	71651168	71650607	71650607	Frame_Shift_Del	A	-	p.R1321fs
LIHC	TCGA-DD-A3A0-01	exon_skip_326432	71649944	71651168	71650776	71650776	Frame_Shift_Del	A	-	p.K1378fs
LIHC	TCGA-DD-A3A0-01	exon_skip_326432	71649944	71651168	71650996	71650996	Frame_Shift_Del	A	-	p.E1451fs
HNSC	TCGA-CV-7407-01	exon_skip_326437	71653590	71654544	71653593	71653596	Frame_Shift_Del	CCAT	-	p.P1532fs
HNSC	TCGA-CV-7407-01	exon_skip_326437	71653590	71654544	71653593	71653596	Frame_Shift_Del	CCAT	-	p.PL1532fs
LIHC	TCGA-DD-A1EG-01	exon_skip_326437	71653590	71654544	71653924	71653924	Frame_Shift_Del	T	-	p.L1642fs
LIHC	TCGA-G3-A3CJ-01	exon_skip_326437	71653590	71654544	71653924	71653924	Frame_Shift_Del	T	-	p.L1642fs
LIHC	TCGA-G3-A3CJ-01	exon_skip_326437	71653590	71654544	71654270	71654270	Frame_Shift_Del	G	-	p.E1757fs
LIHC	TCGA-DD-A1EG-01	exon_skip_326437	71653590	71654544	71654304	71654304	Frame_Shift_Del	A	-	p.K1769fs
LIHC	TCGA-DD-A1EG-01	exon_skip_326446 exon_skip_326448	71655661	71655781	71655725	71655725	Frame_Shift_Del	A	-	p.E1865fs
LIHC	TCGA-DD-A1EG-01	exon_skip_326446 exon_skip_326448	71655677	71655781	71655725	71655725	Frame_Shift_Del	A	-	p.E1865fs
LIHC	TCGA-DD-A39Y-01	exon_skip_326451	71658457	71658558	71658531	71658531	Frame_Shift_Del	A	-	p.K1909fs
LIHC	TCGA-BC-A112-01	exon_skip_326432	71649944	71651168	71650707	71650708	Frame_Shift_Ins	-	A	p.K1355fs
LUAD	TCGA-55-A4DG-01	exon_skip_326406	71575557	71577401	71576136	71576136	Nonsense_Mutation	C	T	p.R18*
LUAD	TCGA-55-A4DG-01	exon_skip_326401 exon_skip_326412	71575883	71577401	71576136	71576136	Nonsense_Mutation	C	T	p.R18*
SKCM	TCGA-EE-A2MJ-06	exon_skip_326406	71575557	71577401	71576268	71576268	Nonsense_Mutation	C	T	p.Q62*
SKCM	TCGA-EE-A2MJ-06	exon_skip_326401 exon_skip_326412	71575883	71577401	71576268	71576268	Nonsense_Mutation	C	T	p.Q62*
SKCM	TCGA-W3-A828-06	exon_skip_326406	71575557	71577401	71576396	71576396	Nonsense_Mutation	G	A	p.W104*
SKCM	TCGA-W3-A828-06	exon_skip_326401 exon_skip_326412	71575883	71577401	71576396	71576396	Nonsense_Mutation	G	A	p.W104*
SKCM	TCGA-ER-A19W-06	exon_skip_326406	71575557	71577401	71576658	71576658	Nonsense_Mutation	C	T	p.Q192*
SKCM	TCGA-ER-A19W-06	exon_skip_326401 exon_skip_326412	71575883	71577401	71576658	71576658	Nonsense_Mutation	C	T	p.Q192*
SKCM	TCGA-EE-A29D-06	exon_skip_326406	71575557	71577401	71576895	71576895	Nonsense_Mutation	C	T	p.Q271*
SKCM	TCGA-EE-A29D-06	exon_skip_326401 exon_skip_326412	71575883	71577401	71576895	71576895	Nonsense_Mutation	C	T	p.Q271*
UCEC	TCGA-D1-A16X-01	exon_skip_326419	71591084	71591382	71591334	71591334	Nonsense_Mutation	C	T	p.R557*
READ	TCGA-AG-A002-01	exon_skip_326432	71649944	71651168	71650056	71650056	Nonsense_Mutation	G	T	p.E1138X
LUAD	TCGA-93-A4JQ-01	exon_skip_326432	71649944	71651168	71650870	71650870	Nonsense_Mutation	C	G	p.S1409*
STAD	TCGA-BR-8680-01	exon_skip_326437	71653590	71654544	71653942	71653942	Nonsense_Mutation	T	G	p.L1648*
STAD	TCGA-BR-8680-01	exon_skip_326437	71653590	71654544	71653942	71653942	Nonsense_Mutation	T	G	p.L1648X
LUAD	TCGA-50-5930-01	exon_skip_326437	71653590	71654544	71654172	71654172	Nonsense_Mutation	C	T	p.Q1725*
UCEC	TCGA-B5-A11E-01	exon_skip_326446 exon_skip_326448	71655661	71655781	71655769	71655769	Nonsense_Mutation	C	T	p.Q1880*
UCEC	TCGA-B5-A11E-01	exon_skip_326446 exon_skip_326448	71655677	71655781	71655769	71655769	Nonsense_Mutation	C	T	p.Q1880*
BLCA	TCGA-XF-AAMG-01	exon_skip_326451	71658457	71658558	71658555	71658555	Nonsense_Mutation	G	T	p.E1917*

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

Depth of coverage in three exons	Mutation description
	Sample: TCGA-B5-A11E-01
	Cancer type: UCEC
	ESID: exon_skip_326448
	Skipped exon start: 71655661
	Skipped exon end: 71655781
	Mutation start: 71655769
	Mutation end: 71655769
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q1880*
	Sample: TCGA-B5-A11E-01
	Cancer type: UCEC
	ESID: exon_skip_326448
	Skipped exon start: 71655677
	Skipped exon end: 71655781
	Mutation start: 71655769
	Mutation end: 71655769
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q1880*
exon_skip_104037_UCEC_TCGA-B5-A11E-01.png
exon_skip_106242_UCEC_TCGA-B5-A11E-01.png
exon_skip_108777_UCEC_TCGA-B5-A11E-01.png
exon_skip_108778_UCEC_TCGA-B5-A11E-01.png
exon_skip_121584_UCEC_TCGA-B5-A11E-01.png
exon_skip_121649_UCEC_TCGA-B5-A11E-01.png
exon_skip_131821_UCEC_TCGA-B5-A11E-01.png
exon_skip_133126_UCEC_TCGA-B5-A11E-01.png
exon_skip_23327_UCEC_TCGA-B5-A11E-01.png
exon_skip_27874_UCEC_TCGA-B5-A11E-01.png
exon_skip_312611_UCEC_TCGA-B5-A11E-01.png
exon_skip_312613_UCEC_TCGA-B5-A11E-01.png
exon_skip_312641_UCEC_TCGA-B5-A11E-01.png
exon_skip_313540_UCEC_TCGA-B5-A11E-01.png
exon_skip_326446_UCEC_TCGA-B5-A11E-01.png
exon_skip_326448_UCEC_TCGA-B5-A11E-01.png
exon_skip_330038_UCEC_TCGA-B5-A11E-01.png
exon_skip_340150_UCEC_TCGA-B5-A11E-01.png
exon_skip_348004_UCEC_TCGA-B5-A11E-01.png
exon_skip_348005_UCEC_TCGA-B5-A11E-01.png
exon_skip_377858_UCEC_TCGA-B5-A11E-01.png
exon_skip_380242_UCEC_TCGA-B5-A11E-01.png
exon_skip_433438_UCEC_TCGA-B5-A11E-01.png
exon_skip_489645_UCEC_TCGA-B5-A11E-01.png
exon_skip_500396_UCEC_TCGA-B5-A11E-01.png
exon_skip_62223_UCEC_TCGA-B5-A11E-01.png
exon_skip_97620_UCEC_TCGA-B5-A11E-01.png
exon_skip_97655_UCEC_TCGA-B5-A11E-01.png
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71653924
	Mutation end: 71653924
	Mutation type: Frame_Shift_Del
	Reference seq: T
	Mutation seq: -
	AAchange: p.L1642fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71654304
	Mutation end: 71654304
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.K1769fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326448
	Skipped exon start: 71655661
	Skipped exon end: 71655781
	Mutation start: 71655725
	Mutation end: 71655725
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1865fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326448
	Skipped exon start: 71655677
	Skipped exon end: 71655781
	Mutation start: 71655725
	Mutation end: 71655725
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1865fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326432
	Skipped exon start: 71649944
	Skipped exon end: 71651168
	Mutation start: 71650549
	Mutation end: 71650549
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1302fs
exon_skip_103075_LIHC_TCGA-DD-A1EG-01.png
exon_skip_100809_LIHC_TCGA-DD-A1EG-01.png
exon_skip_101656_LIHC_TCGA-DD-A1EG-01.png
exon_skip_10700_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_18708_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_99140_LIHC_TCGA-DD-A1EG-01.png
	Sample: TCGA-B5-A11E-01
	Cancer type: UCEC
	ESID: exon_skip_326448
	Skipped exon start: 71655661
	Skipped exon end: 71655781
	Mutation start: 71655769
	Mutation end: 71655769
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q1880*
	Sample: TCGA-B5-A11E-01
	Cancer type: UCEC
	ESID: exon_skip_326448
	Skipped exon start: 71655677
	Skipped exon end: 71655781
	Mutation start: 71655769
	Mutation end: 71655769
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: T
	AAchange: p.Q1880*
exon_skip_104037_UCEC_TCGA-B5-A11E-01.png
exon_skip_106242_UCEC_TCGA-B5-A11E-01.png
exon_skip_108777_UCEC_TCGA-B5-A11E-01.png
exon_skip_108778_UCEC_TCGA-B5-A11E-01.png
exon_skip_121584_UCEC_TCGA-B5-A11E-01.png
exon_skip_121649_UCEC_TCGA-B5-A11E-01.png
exon_skip_131821_UCEC_TCGA-B5-A11E-01.png
exon_skip_133126_UCEC_TCGA-B5-A11E-01.png
exon_skip_23327_UCEC_TCGA-B5-A11E-01.png
exon_skip_27874_UCEC_TCGA-B5-A11E-01.png
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exon_skip_312613_UCEC_TCGA-B5-A11E-01.png
exon_skip_312641_UCEC_TCGA-B5-A11E-01.png
exon_skip_313540_UCEC_TCGA-B5-A11E-01.png
exon_skip_326446_UCEC_TCGA-B5-A11E-01.png
exon_skip_326448_UCEC_TCGA-B5-A11E-01.png
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exon_skip_348004_UCEC_TCGA-B5-A11E-01.png
exon_skip_348005_UCEC_TCGA-B5-A11E-01.png
exon_skip_377858_UCEC_TCGA-B5-A11E-01.png
exon_skip_380242_UCEC_TCGA-B5-A11E-01.png
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exon_skip_500396_UCEC_TCGA-B5-A11E-01.png
exon_skip_62223_UCEC_TCGA-B5-A11E-01.png
exon_skip_97620_UCEC_TCGA-B5-A11E-01.png
exon_skip_97655_UCEC_TCGA-B5-A11E-01.png
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71653924
	Mutation end: 71653924
	Mutation type: Frame_Shift_Del
	Reference seq: T
	Mutation seq: -
	AAchange: p.L1642fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71654304
	Mutation end: 71654304
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.K1769fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326448
	Skipped exon start: 71655661
	Skipped exon end: 71655781
	Mutation start: 71655725
	Mutation end: 71655725
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1865fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326448
	Skipped exon start: 71655677
	Skipped exon end: 71655781
	Mutation start: 71655725
	Mutation end: 71655725
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1865fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326432
	Skipped exon start: 71649944
	Skipped exon end: 71651168
	Mutation start: 71650549
	Mutation end: 71650549
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1302fs
exon_skip_103075_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_3064_LIHC_TCGA-DD-A1EG-01.png
exon_skip_307291_LIHC_TCGA-DD-A1EG-01.png
exon_skip_307292_LIHC_TCGA-DD-A1EG-01.png
exon_skip_30744_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_307495_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_30792_LIHC_TCGA-DD-A1EG-01.png
exon_skip_308209_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_308911_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_320805_LIHC_TCGA-DD-A1EG-01.png
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	Sample: TCGA-BR-8680-01
	Cancer type: STAD
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71653942
	Mutation end: 71653942
	Mutation type: Nonsense_Mutation
	Reference seq: T
	Mutation seq: G
	AAchange: p.L1648X
	Sample: TCGA-BR-8680-01
	Cancer type: STAD
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71653942
	Mutation end: 71653942
	Mutation type: Nonsense_Mutation
	Reference seq: T
	Mutation seq: G
	AAchange: p.L1648*
exon_skip_106946_STAD_TCGA-BR-8680-01.png
exon_skip_107215_STAD_TCGA-BR-8680-01.png
exon_skip_122567_STAD_TCGA-BR-8680-01.png
exon_skip_122573_STAD_TCGA-BR-8680-01.png
exon_skip_144294_STAD_TCGA-BR-8680-01.png
exon_skip_26878_STAD_TCGA-BR-8680-01.png
exon_skip_30156_STAD_TCGA-BR-8680-01.png
exon_skip_324648_STAD_TCGA-BR-8680-01.png
exon_skip_326437_STAD_TCGA-BR-8680-01.png
exon_skip_326558_STAD_TCGA-BR-8680-01.png
exon_skip_326569_STAD_TCGA-BR-8680-01.png
exon_skip_328488_STAD_TCGA-BR-8680-01.png
exon_skip_335090_STAD_TCGA-BR-8680-01.png
exon_skip_389166_STAD_TCGA-BR-8680-01.png
exon_skip_40432_STAD_TCGA-BR-8680-01.png
exon_skip_40460_STAD_TCGA-BR-8680-01.png
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exon_skip_436498_STAD_TCGA-BR-8680-01.png
exon_skip_466512_STAD_TCGA-BR-8680-01.png
exon_skip_478774_STAD_TCGA-BR-8680-01.png
exon_skip_484956_STAD_TCGA-BR-8680-01.png
exon_skip_64135_STAD_TCGA-BR-8680-01.png
exon_skip_64136_STAD_TCGA-BR-8680-01.png
exon_skip_64137_STAD_TCGA-BR-8680-01.png
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exon_skip_69375_STAD_TCGA-BR-8680-01.png
exon_skip_75101_STAD_TCGA-BR-8680-01.png
	Sample: TCGA-CV-7407-01
	Cancer type: HNSC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71653593
	Mutation end: 71653596
	Mutation type: Frame_Shift_Del
	Reference seq: CCAT
	Mutation seq: -
	AAchange: p.PL1532fs
	Sample: TCGA-CV-7407-01
	Cancer type: HNSC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71653593
	Mutation end: 71653596
	Mutation type: Frame_Shift_Del
	Reference seq: CCAT
	Mutation seq: -
	AAchange: p.P1532fs
exon_skip_326437_HNSC_TCGA-CV-7407-01.png
exon_skip_360566_HNSC_TCGA-CV-7407-01.png
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71653924
	Mutation end: 71653924
	Mutation type: Frame_Shift_Del
	Reference seq: T
	Mutation seq: -
	AAchange: p.L1642fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71654304
	Mutation end: 71654304
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.K1769fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326448
	Skipped exon start: 71655661
	Skipped exon end: 71655781
	Mutation start: 71655725
	Mutation end: 71655725
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1865fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326448
	Skipped exon start: 71655677
	Skipped exon end: 71655781
	Mutation start: 71655725
	Mutation end: 71655725
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1865fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326432
	Skipped exon start: 71649944
	Skipped exon end: 71651168
	Mutation start: 71650549
	Mutation end: 71650549
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1302fs
exon_skip_103075_LIHC_TCGA-DD-A1EG-01.png
exon_skip_100809_LIHC_TCGA-DD-A1EG-01.png
exon_skip_101656_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_135741_LIHC_TCGA-DD-A1EG-01.png
exon_skip_135763_LIHC_TCGA-DD-A1EG-01.png
exon_skip_135820_LIHC_TCGA-DD-A1EG-01.png
exon_skip_13608_LIHC_TCGA-DD-A1EG-01.png
exon_skip_138255_LIHC_TCGA-DD-A1EG-01.png
exon_skip_138373_LIHC_TCGA-DD-A1EG-01.png
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	Sample: TCGA-93-A4JQ-01
	Cancer type: LUAD
	ESID: exon_skip_326432
	Skipped exon start: 71649944
	Skipped exon end: 71651168
	Mutation start: 71650870
	Mutation end: 71650870
	Mutation type: Nonsense_Mutation
	Reference seq: C
	Mutation seq: G
	AAchange: p.S1409*
exon_skip_326432_LUAD_TCGA-93-A4JQ-01.png
	Sample: TCGA-BC-A112-01
	Cancer type: LIHC
	ESID: exon_skip_326432
	Skipped exon start: 71649944
	Skipped exon end: 71651168
	Mutation start: 71650707
	Mutation end: 71650708
	Mutation type: Frame_Shift_Ins
	Reference seq: -
	Mutation seq: A
	AAchange: p.K1355fs
exon_skip_114200_LIHC_TCGA-BC-A112-01.png
exon_skip_131894_LIHC_TCGA-BC-A112-01.png
exon_skip_135820_LIHC_TCGA-BC-A112-01.png
exon_skip_138911_LIHC_TCGA-BC-A112-01.png
exon_skip_141587_LIHC_TCGA-BC-A112-01.png
exon_skip_142606_LIHC_TCGA-BC-A112-01.png
exon_skip_146695_LIHC_TCGA-BC-A112-01.png
exon_skip_146697_LIHC_TCGA-BC-A112-01.png
exon_skip_152962_LIHC_TCGA-BC-A112-01.png
exon_skip_155765_LIHC_TCGA-BC-A112-01.png
exon_skip_1757_LIHC_TCGA-BC-A112-01.png
exon_skip_1879_LIHC_TCGA-BC-A112-01.png
exon_skip_1881_LIHC_TCGA-BC-A112-01.png
exon_skip_266_LIHC_TCGA-BC-A112-01.png
exon_skip_284527_LIHC_TCGA-BC-A112-01.png
exon_skip_286998_LIHC_TCGA-BC-A112-01.png
exon_skip_293546_LIHC_TCGA-BC-A112-01.png
exon_skip_293549_LIHC_TCGA-BC-A112-01.png
exon_skip_306900_LIHC_TCGA-BC-A112-01.png
exon_skip_311841_LIHC_TCGA-BC-A112-01.png
exon_skip_325884_LIHC_TCGA-BC-A112-01.png
exon_skip_326432_LIHC_TCGA-BC-A112-01.png
exon_skip_32825_LIHC_TCGA-BC-A112-01.png
exon_skip_331787_LIHC_TCGA-BC-A112-01.png
exon_skip_337208_LIHC_TCGA-BC-A112-01.png
exon_skip_337747_LIHC_TCGA-BC-A112-01.png
exon_skip_339045_LIHC_TCGA-BC-A112-01.png
exon_skip_344031_LIHC_TCGA-BC-A112-01.png
exon_skip_35548_LIHC_TCGA-BC-A112-01.png
exon_skip_35556_LIHC_TCGA-BC-A112-01.png
exon_skip_359720_LIHC_TCGA-BC-A112-01.png
exon_skip_37056_LIHC_TCGA-BC-A112-01.png
exon_skip_37483_LIHC_TCGA-BC-A112-01.png
exon_skip_37491_LIHC_TCGA-BC-A112-01.png
exon_skip_375724_LIHC_TCGA-BC-A112-01.png
exon_skip_378789_LIHC_TCGA-BC-A112-01.png
exon_skip_386291_LIHC_TCGA-BC-A112-01.png
exon_skip_41850_LIHC_TCGA-BC-A112-01.png
exon_skip_435931_LIHC_TCGA-BC-A112-01.png
exon_skip_436296_LIHC_TCGA-BC-A112-01.png
exon_skip_438393_LIHC_TCGA-BC-A112-01.png
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exon_skip_444190_LIHC_TCGA-BC-A112-01.png
exon_skip_44538_LIHC_TCGA-BC-A112-01.png
exon_skip_449944_LIHC_TCGA-BC-A112-01.png
exon_skip_458520_LIHC_TCGA-BC-A112-01.png
exon_skip_460075_LIHC_TCGA-BC-A112-01.png
exon_skip_472635_LIHC_TCGA-BC-A112-01.png
exon_skip_489149_LIHC_TCGA-BC-A112-01.png
exon_skip_492152_LIHC_TCGA-BC-A112-01.png
exon_skip_49506_LIHC_TCGA-BC-A112-01.png
exon_skip_5044_LIHC_TCGA-BC-A112-01.png
exon_skip_512559_LIHC_TCGA-BC-A112-01.png
exon_skip_514460_LIHC_TCGA-BC-A112-01.png
exon_skip_514990_LIHC_TCGA-BC-A112-01.png
exon_skip_55171_LIHC_TCGA-BC-A112-01.png
exon_skip_55175_LIHC_TCGA-BC-A112-01.png
exon_skip_56847_LIHC_TCGA-BC-A112-01.png
exon_skip_57586_LIHC_TCGA-BC-A112-01.png
exon_skip_57892_LIHC_TCGA-BC-A112-01.png
exon_skip_58035_LIHC_TCGA-BC-A112-01.png
exon_skip_6399_LIHC_TCGA-BC-A112-01.png
exon_skip_77132_LIHC_TCGA-BC-A112-01.png
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71653924
	Mutation end: 71653924
	Mutation type: Frame_Shift_Del
	Reference seq: T
	Mutation seq: -
	AAchange: p.L1642fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326437
	Skipped exon start: 71653590
	Skipped exon end: 71654544
	Mutation start: 71654304
	Mutation end: 71654304
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.K1769fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326448
	Skipped exon start: 71655661
	Skipped exon end: 71655781
	Mutation start: 71655725
	Mutation end: 71655725
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1865fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326448
	Skipped exon start: 71655677
	Skipped exon end: 71655781
	Mutation start: 71655725
	Mutation end: 71655725
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1865fs
	Sample: TCGA-DD-A1EG-01
	Cancer type: LIHC
	ESID: exon_skip_326432
	Skipped exon start: 71649944
	Skipped exon end: 71651168
	Mutation start: 71650549
	Mutation end: 71650549
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1302fs
exon_skip_103075_LIHC_TCGA-DD-A1EG-01.png
exon_skip_100809_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_115587_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_131505_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_13608_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_138373_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_443104_LIHC_TCGA-DD-A1EG-01.png
exon_skip_443977_LIHC_TCGA-DD-A1EG-01.png
exon_skip_443978_LIHC_TCGA-DD-A1EG-01.png
exon_skip_444190_LIHC_TCGA-DD-A1EG-01.png
exon_skip_444765_LIHC_TCGA-DD-A1EG-01.png
exon_skip_445559_LIHC_TCGA-DD-A1EG-01.png
exon_skip_446492_LIHC_TCGA-DD-A1EG-01.png
exon_skip_446495_LIHC_TCGA-DD-A1EG-01.png
exon_skip_449536_LIHC_TCGA-DD-A1EG-01.png
exon_skip_449592_LIHC_TCGA-DD-A1EG-01.png
exon_skip_4499_LIHC_TCGA-DD-A1EG-01.png
exon_skip_450058_LIHC_TCGA-DD-A1EG-01.png
exon_skip_450540_LIHC_TCGA-DD-A1EG-01.png
exon_skip_451867_LIHC_TCGA-DD-A1EG-01.png
exon_skip_456736_LIHC_TCGA-DD-A1EG-01.png
exon_skip_457729_LIHC_TCGA-DD-A1EG-01.png
exon_skip_457730_LIHC_TCGA-DD-A1EG-01.png
exon_skip_457842_LIHC_TCGA-DD-A1EG-01.png
exon_skip_459148_LIHC_TCGA-DD-A1EG-01.png
exon_skip_462138_LIHC_TCGA-DD-A1EG-01.png
exon_skip_466984_LIHC_TCGA-DD-A1EG-01.png
exon_skip_467199_LIHC_TCGA-DD-A1EG-01.png
exon_skip_467371_LIHC_TCGA-DD-A1EG-01.png
exon_skip_467372_LIHC_TCGA-DD-A1EG-01.png
exon_skip_46817_LIHC_TCGA-DD-A1EG-01.png
exon_skip_471387_LIHC_TCGA-DD-A1EG-01.png
exon_skip_471458_LIHC_TCGA-DD-A1EG-01.png
exon_skip_472013_LIHC_TCGA-DD-A1EG-01.png
exon_skip_472955_LIHC_TCGA-DD-A1EG-01.png
exon_skip_473416_LIHC_TCGA-DD-A1EG-01.png
exon_skip_475734_LIHC_TCGA-DD-A1EG-01.png
exon_skip_476238_LIHC_TCGA-DD-A1EG-01.png
exon_skip_476392_LIHC_TCGA-DD-A1EG-01.png
exon_skip_476535_LIHC_TCGA-DD-A1EG-01.png
exon_skip_478361_LIHC_TCGA-DD-A1EG-01.png
exon_skip_47845_LIHC_TCGA-DD-A1EG-01.png
exon_skip_483792_LIHC_TCGA-DD-A1EG-01.png
exon_skip_483806_LIHC_TCGA-DD-A1EG-01.png
exon_skip_484511_LIHC_TCGA-DD-A1EG-01.png
exon_skip_486903_LIHC_TCGA-DD-A1EG-01.png
exon_skip_486908_LIHC_TCGA-DD-A1EG-01.png
exon_skip_487634_LIHC_TCGA-DD-A1EG-01.png
exon_skip_48914_LIHC_TCGA-DD-A1EG-01.png
exon_skip_489575_LIHC_TCGA-DD-A1EG-01.png
exon_skip_489706_LIHC_TCGA-DD-A1EG-01.png
exon_skip_490514_LIHC_TCGA-DD-A1EG-01.png
exon_skip_492073_LIHC_TCGA-DD-A1EG-01.png
exon_skip_494000_LIHC_TCGA-DD-A1EG-01.png
exon_skip_495598_LIHC_TCGA-DD-A1EG-01.png
exon_skip_495600_LIHC_TCGA-DD-A1EG-01.png
exon_skip_497719_LIHC_TCGA-DD-A1EG-01.png
exon_skip_498628_LIHC_TCGA-DD-A1EG-01.png
exon_skip_498631_LIHC_TCGA-DD-A1EG-01.png
exon_skip_499018_LIHC_TCGA-DD-A1EG-01.png
exon_skip_501551_LIHC_TCGA-DD-A1EG-01.png
exon_skip_503330_LIHC_TCGA-DD-A1EG-01.png
exon_skip_503777_LIHC_TCGA-DD-A1EG-01.png
exon_skip_504288_LIHC_TCGA-DD-A1EG-01.png
exon_skip_5044_LIHC_TCGA-DD-A1EG-01.png
exon_skip_506320_LIHC_TCGA-DD-A1EG-01.png
exon_skip_507513_LIHC_TCGA-DD-A1EG-01.png
exon_skip_508970_LIHC_TCGA-DD-A1EG-01.png
exon_skip_510119_LIHC_TCGA-DD-A1EG-01.png
exon_skip_512244_LIHC_TCGA-DD-A1EG-01.png
exon_skip_512530_LIHC_TCGA-DD-A1EG-01.png
exon_skip_513207_LIHC_TCGA-DD-A1EG-01.png
exon_skip_513240_LIHC_TCGA-DD-A1EG-01.png
exon_skip_514990_LIHC_TCGA-DD-A1EG-01.png
exon_skip_516934_LIHC_TCGA-DD-A1EG-01.png
exon_skip_517296_LIHC_TCGA-DD-A1EG-01.png
exon_skip_517308_LIHC_TCGA-DD-A1EG-01.png
exon_skip_52417_LIHC_TCGA-DD-A1EG-01.png
exon_skip_54123_LIHC_TCGA-DD-A1EG-01.png
exon_skip_54476_LIHC_TCGA-DD-A1EG-01.png
exon_skip_56470_LIHC_TCGA-DD-A1EG-01.png
exon_skip_57633_LIHC_TCGA-DD-A1EG-01.png
exon_skip_57892_LIHC_TCGA-DD-A1EG-01.png
exon_skip_57897_LIHC_TCGA-DD-A1EG-01.png
exon_skip_58035_LIHC_TCGA-DD-A1EG-01.png
exon_skip_5818_LIHC_TCGA-DD-A1EG-01.png
exon_skip_58444_LIHC_TCGA-DD-A1EG-01.png
exon_skip_58894_LIHC_TCGA-DD-A1EG-01.png
exon_skip_59424_LIHC_TCGA-DD-A1EG-01.png
exon_skip_59476_LIHC_TCGA-DD-A1EG-01.png
exon_skip_59654_LIHC_TCGA-DD-A1EG-01.png
exon_skip_60187_LIHC_TCGA-DD-A1EG-01.png
exon_skip_60189_LIHC_TCGA-DD-A1EG-01.png
exon_skip_62322_LIHC_TCGA-DD-A1EG-01.png
exon_skip_63747_LIHC_TCGA-DD-A1EG-01.png
exon_skip_66185_LIHC_TCGA-DD-A1EG-01.png
exon_skip_66376_LIHC_TCGA-DD-A1EG-01.png
exon_skip_66813_LIHC_TCGA-DD-A1EG-01.png
exon_skip_67402_LIHC_TCGA-DD-A1EG-01.png
exon_skip_67594_LIHC_TCGA-DD-A1EG-01.png
exon_skip_67918_LIHC_TCGA-DD-A1EG-01.png
exon_skip_68288_LIHC_TCGA-DD-A1EG-01.png
exon_skip_68407_LIHC_TCGA-DD-A1EG-01.png
exon_skip_68411_LIHC_TCGA-DD-A1EG-01.png
exon_skip_68522_LIHC_TCGA-DD-A1EG-01.png
exon_skip_68768_LIHC_TCGA-DD-A1EG-01.png
exon_skip_69056_LIHC_TCGA-DD-A1EG-01.png
exon_skip_70050_LIHC_TCGA-DD-A1EG-01.png
exon_skip_71400_LIHC_TCGA-DD-A1EG-01.png
exon_skip_77097_LIHC_TCGA-DD-A1EG-01.png
exon_skip_79815_LIHC_TCGA-DD-A1EG-01.png
exon_skip_81531_LIHC_TCGA-DD-A1EG-01.png
exon_skip_81532_LIHC_TCGA-DD-A1EG-01.png
exon_skip_822_LIHC_TCGA-DD-A1EG-01.png
exon_skip_82890_LIHC_TCGA-DD-A1EG-01.png
exon_skip_84090_LIHC_TCGA-DD-A1EG-01.png
exon_skip_86135_LIHC_TCGA-DD-A1EG-01.png
exon_skip_87721_LIHC_TCGA-DD-A1EG-01.png
exon_skip_87_LIHC_TCGA-DD-A1EG-01.png
exon_skip_93888_LIHC_TCGA-DD-A1EG-01.png
exon_skip_93891_LIHC_TCGA-DD-A1EG-01.png
exon_skip_94866_LIHC_TCGA-DD-A1EG-01.png
exon_skip_96939_LIHC_TCGA-DD-A1EG-01.png
exon_skip_9694_LIHC_TCGA-DD-A1EG-01.png
exon_skip_97667_LIHC_TCGA-DD-A1EG-01.png
exon_skip_98055_LIHC_TCGA-DD-A1EG-01.png
exon_skip_98056_LIHC_TCGA-DD-A1EG-01.png
exon_skip_99140_LIHC_TCGA-DD-A1EG-01.png
	Sample: TCGA-86-A4JF-01
	Cancer type: LUAD
	ESID: exon_skip_326432
	Skipped exon start: 71649944
	Skipped exon end: 71651168
	Mutation start: 71650549
	Mutation end: 71650549
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.E1302fs
exon_skip_286384_LUAD_TCGA-86-A4JF-01.png
exon_skip_307494_LUAD_TCGA-86-A4JF-01.png
exon_skip_307495_LUAD_TCGA-86-A4JF-01.png
exon_skip_326432_LUAD_TCGA-86-A4JF-01.png
	Sample: TCGA-BR-4201-01
	Cancer type: STAD
	ESID: exon_skip_326432
	Skipped exon start: 71649944
	Skipped exon end: 71651168
	Mutation start: 71649954
	Mutation end: 71649954
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.L1103fs
exon_skip_141192_STAD_TCGA-BR-4201-01.png
exon_skip_16960_STAD_TCGA-BR-4201-01.png
exon_skip_326432_STAD_TCGA-BR-4201-01.png
exon_skip_337819_STAD_TCGA-BR-4201-01.png
exon_skip_345944_STAD_TCGA-BR-4201-01.png
exon_skip_345950_STAD_TCGA-BR-4201-01.png
exon_skip_351676_STAD_TCGA-BR-4201-01.png
exon_skip_454428_STAD_TCGA-BR-4201-01.png
exon_skip_454431_STAD_TCGA-BR-4201-01.png
exon_skip_454433_STAD_TCGA-BR-4201-01.png
exon_skip_45525_STAD_TCGA-BR-4201-01.png
exon_skip_456626_STAD_TCGA-BR-4201-01.png
exon_skip_494729_STAD_TCGA-BR-4201-01.png
exon_skip_60290_STAD_TCGA-BR-4201-01.png
exon_skip_60294_STAD_TCGA-BR-4201-01.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
BICR18_UPPER_AERODIGESTIVE_TRACT	71575883	71577401	71576114	71576114	Frame_Shift_Del	A	-	p.G10fs
BICR18_UPPER_AERODIGESTIVE_TRACT	71575557	71577401	71576114	71576114	Frame_Shift_Del	A	-	p.G10fs
SNU719_STOMACH	71575883	71577401	71577038	71577041	Frame_Shift_Del	AGTT	-	p.TV318fs
SNU719_STOMACH	71575557	71577401	71577038	71577041	Frame_Shift_Del	AGTT	-	p.TV318fs
ST486_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71575883	71577401	71577274	71577275	Frame_Shift_Del	CA	-	p.S397fs
ST486_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71575557	71577401	71577274	71577275	Frame_Shift_Del	CA	-	p.S397fs
SKMEL2_SKIN	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
SNUC4_LARGE_INTESTINE	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
A375_SKIN	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
AN3CA_ENDOMETRIUM	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
LS411N_LARGE_INTESTINE	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
CL34_LARGE_INTESTINE	71649944	71651168	71650549	71650549	Frame_Shift_Del	A	-	p.E1302fs
BICR18_UPPER_AERODIGESTIVE_TRACT	71575883	71577401	71576116	71576117	Frame_Shift_Ins	-	C	p.F12fs
BICR18_UPPER_AERODIGESTIVE_TRACT	71575557	71577401	71576116	71576117	Frame_Shift_Ins	-	C	p.F12fs
SNU1_STOMACH	71649944	71651168	71650440	71650441	Frame_Shift_Ins	-	A	p.E1266fs
CW2_LARGE_INTESTINE	71649944	71651168	71650548	71650549	Frame_Shift_Ins	-	A	p.E1302fs
OCUBM_BREAST	71653590	71654544	71654446	71654447	Frame_Shift_Ins	-	A	p.TK1816fs
CAL54_KIDNEY	71653590	71654544	71654446	71654447	Frame_Shift_Ins	-	A	p.TK1816fs
JMSU1_URINARY_TRACT	71653590	71654544	71654446	71654447	Frame_Shift_Ins	-	A	p.TK1816fs
MDST8_LARGE_INTESTINE	71653590	71654544	71654446	71654447	Frame_Shift_Ins	-	A	p.TK1816fs
SNU668_STOMACH	71653590	71654544	71654446	71654447	Frame_Shift_Ins	-	A	p.TK1816fs
HMVII_SKIN	71575883	71577401	71577221	71577232	In_Frame_Del	TCCCATTCGGTC	-	p.PIRS380del
HMVII_SKIN	71575557	71577401	71577221	71577232	In_Frame_Del	TCCCATTCGGTC	-	p.PIRS380del
MUTZ5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71591084	71591382	71591264	71591269	In_Frame_Del	CAGATC	-	p.RS540del
HCC15_LUNG	71575883	71577401	71576113	71576113	Missense_Mutation	G	T	p.G10V
HCC15_LUNG	71575557	71577401	71576113	71576113	Missense_Mutation	G	T	p.G10V
HS870T_FIBROBLAST	71575883	71577401	71576257	71576257	Missense_Mutation	A	G	p.H58R
HS870T_FIBROBLAST	71575557	71577401	71576257	71576257	Missense_Mutation	A	G	p.H58R
BFTC905_URINARY_TRACT	71575883	71577401	71576301	71576301	Missense_Mutation	G	A	p.V73I
BFTC905_URINARY_TRACT	71575557	71577401	71576301	71576301	Missense_Mutation	G	A	p.V73I
NCIH1105_LUNG	71575883	71577401	71576373	71576373	Missense_Mutation	G	T	p.G97W
NCIH1105_LUNG	71575557	71577401	71576373	71576373	Missense_Mutation	G	T	p.G97W
SNUC2A_LARGE_INTESTINE	71575883	71577401	71576392	71576392	Missense_Mutation	G	A	p.R103Q
SNUC2A_LARGE_INTESTINE	71575557	71577401	71576392	71576392	Missense_Mutation	G	A	p.R103Q
SNUC2B_LARGE_INTESTINE	71575883	71577401	71576392	71576392	Missense_Mutation	G	A	p.R103Q
SNUC2B_LARGE_INTESTINE	71575557	71577401	71576392	71576392	Missense_Mutation	G	A	p.R103Q
NCIH1563_LUNG	71575883	71577401	71576422	71576422	Missense_Mutation	C	T	p.S113L
NCIH1563_LUNG	71575557	71577401	71576422	71576422	Missense_Mutation	C	T	p.S113L
NCIH460_LUNG	71575883	71577401	71576566	71576566	Missense_Mutation	C	T	p.P161L
NCIH460_LUNG	71575557	71577401	71576566	71576566	Missense_Mutation	C	T	p.P161L
ABC1_LUNG	71575883	71577401	71576638	71576638	Missense_Mutation	G	A	p.R185Q
ABC1_LUNG	71575557	71577401	71576638	71576638	Missense_Mutation	G	A	p.R185Q
NCIH1568_LUNG	71575883	71577401	71576653	71576653	Missense_Mutation	C	G	p.P190R
NCIH1568_LUNG	71575557	71577401	71576653	71576653	Missense_Mutation	C	G	p.P190R
RH41_SOFT_TISSUE	71575883	71577401	71576656	71576656	Missense_Mutation	C	T	p.S191F
RH41_SOFT_TISSUE	71575557	71577401	71576656	71576656	Missense_Mutation	C	T	p.S191F
EB1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71575883	71577401	71576740	71576740	Missense_Mutation	A	G	p.Y219C
EB1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71575557	71577401	71576740	71576740	Missense_Mutation	A	G	p.Y219C
GP2D_LARGE_INTESTINE	71575883	71577401	71576761	71576761	Missense_Mutation	T	C	p.V226A
GP2D_LARGE_INTESTINE	71575557	71577401	71576761	71576761	Missense_Mutation	T	C	p.V226A
GP5D_LARGE_INTESTINE	71575883	71577401	71576761	71576761	Missense_Mutation	T	C	p.V226A
GP5D_LARGE_INTESTINE	71575557	71577401	71576761	71576761	Missense_Mutation	T	C	p.V226A
SNU1272_KIDNEY	71575883	71577401	71576799	71576799	Missense_Mutation	G	A	p.E239K
SNU1272_KIDNEY	71575557	71577401	71576799	71576799	Missense_Mutation	G	A	p.E239K
CW2_LARGE_INTESTINE	71575883	71577401	71576832	71576832	Missense_Mutation	G	A	p.A250T
CW2_LARGE_INTESTINE	71575557	71577401	71576832	71576832	Missense_Mutation	G	A	p.A250T
KGN_OVARY	71575883	71577401	71576893	71576893	Missense_Mutation	G	A	p.R270H
KGN_OVARY	71575557	71577401	71576893	71576893	Missense_Mutation	G	A	p.R270H
SCLC22H_LUNG	71575883	71577401	71576901	71576901	Missense_Mutation	G	T	p.D273Y
SCLC22H_LUNG	71575557	71577401	71576901	71576901	Missense_Mutation	G	T	p.D273Y
SCLC21H_LUNG	71575883	71577401	71576901	71576901	Missense_Mutation	G	T	p.D273Y
SCLC21H_LUNG	71575557	71577401	71576901	71576901	Missense_Mutation	G	T	p.D273Y
TO175T_FIBROBLAST	71575883	71577401	71576976	71576976	Missense_Mutation	A	G	p.I298V
TO175T_FIBROBLAST	71575557	71577401	71576976	71576976	Missense_Mutation	A	G	p.I298V
SARC9371_BONE	71575883	71577401	71576997	71576997	Missense_Mutation	C	T	p.L305F
SARC9371_BONE	71575557	71577401	71576997	71576997	Missense_Mutation	C	T	p.L305F
WM88_SKIN	71575883	71577401	71577013	71577013	Missense_Mutation	C	T	p.S310F
WM88_SKIN	71575557	71577401	71577013	71577013	Missense_Mutation	C	T	p.S310F
MDAMB453_BREAST	71575883	71577401	71577057	71577057	Missense_Mutation	C	G	p.Q325E
MDAMB453_BREAST	71575557	71577401	71577057	71577057	Missense_Mutation	C	G	p.Q325E
KARPAS422_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71575883	71577401	71577246	71577246	Missense_Mutation	G	A	p.V388M
KARPAS422_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71575557	71577401	71577246	71577246	Missense_Mutation	G	A	p.V388M
639V_URINARY_TRACT	71575883	71577401	71577268	71577268	Missense_Mutation	A	T	p.K395M
639V_URINARY_TRACT	71575557	71577401	71577268	71577268	Missense_Mutation	A	T	p.K395M
SNU245_BILIARY_TRACT	71575883	71577401	71577282	71577282	Missense_Mutation	G	A	p.D400N
SNU245_BILIARY_TRACT	71575557	71577401	71577282	71577282	Missense_Mutation	G	A	p.D400N
EN_ENDOMETRIUM	71575883	71577401	71577390	71577390	Missense_Mutation	A	G	p.S436G
EN_ENDOMETRIUM	71575557	71577401	71577390	71577390	Missense_Mutation	A	G	p.S436G
MN60_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71591084	71591382	71591119	71591119	Missense_Mutation	G	A	p.R485Q
NCIH2172_LUNG	71591084	71591382	71591122	71591122	Missense_Mutation	G	C	p.R486T
TGBC24TKB_BILIARY_TRACT	71591084	71591382	71591167	71591167	Missense_Mutation	C	T	p.S501L
MAC2A_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71591084	71591382	71591181	71591181	Missense_Mutation	C	T	p.R506C
DETROIT562_UPPER_AERODIGESTIVE_TRACT	71591084	71591382	71591185	71591185	Missense_Mutation	G	A	p.R507Q
DOV13_OVARY	71591084	71591382	71591201	71591201	Missense_Mutation	G	A	p.M512I
HEC265_ENDOMETRIUM	71591084	71591382	71591218	71591218	Missense_Mutation	C	T	p.P518L
HCC2998_LARGE_INTESTINE	71591084	71591382	71591296	71591296	Missense_Mutation	G	A	p.R544Q
EW24_BONE	71591084	71591382	71591317	71591317	Missense_Mutation	G	T	p.G551V
SNU81_LARGE_INTESTINE	71595512	71595658	71595515	71595515	Missense_Mutation	C	T	p.R667W
MUGCHOR1_BONE	71595512	71595658	71595516	71595516	Missense_Mutation	G	T	p.R667L
D542MG_CENTRAL_NERVOUS_SYSTEM	71595512	71595658	71595593	71595593	Missense_Mutation	G	A	p.V693M
L542_MATCHED_NORMAL_TISSUE	71595512	71595658	71595593	71595593	Missense_Mutation	G	A	p.V693M
TUHR4TKB_KIDNEY	71595512	71595658	71595615	71595615	Missense_Mutation	T	C	p.F700S
SNU81_LARGE_INTESTINE	71635252	71635377	71635258	71635258	Missense_Mutation	C	A	p.L1048I
LOUNH91_LUNG	71635252	71635377	71635267	71635267	Missense_Mutation	G	C	p.D1051H
HEC1A_ENDOMETRIUM	71635252	71635377	71635298	71635298	Missense_Mutation	G	T	p.S1061I
LIM1215_LARGE_INTESTINE	71649944	71651168	71650163	71650163	Missense_Mutation	G	T	p.E1173D
CW2_LARGE_INTESTINE	71649944	71651168	71650177	71650177	Missense_Mutation	T	C	p.I1178T
HCC1833_LUNG	71649944	71651168	71650249	71650249	Missense_Mutation	A	G	p.Q1202R
A253_SALIVARY_GLAND	71649944	71651168	71650284	71650284	Missense_Mutation	G	A	p.A1214T
JHUEM7_ENDOMETRIUM	71649944	71651168	71650332	71650332	Missense_Mutation	T	C	p.F1230L
FTC238_THYROID	71649944	71651168	71650465	71650465	Missense_Mutation	T	C	p.I1274T
NCIH1930_LUNG	71649944	71651168	71650480	71650480	Missense_Mutation	G	T	p.C1279F
BCPAP_THYROID	71649944	71651168	71650568	71650568	Missense_Mutation	T	G	p.D1308E
MDAMB415_BREAST	71649944	71651168	71650624	71650624	Missense_Mutation	G	A	p.G1327E
MDAMB415_BREAST	71649944	71651168	71650629	71650629	Missense_Mutation	G	A	p.E1329K
BEN_LUNG	71649944	71651168	71650643	71650643	Missense_Mutation	G	C	p.K1333N
A498_KIDNEY	71649944	71651168	71650712	71650712	Missense_Mutation	C	G	p.N1356K
NCIH2170_LUNG	71649944	71651168	71650747	71650747	Missense_Mutation	G	A	p.G1368D
CMLT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	71649944	71651168	71650782	71650782	Missense_Mutation	A	G	p.S1380G
JHOS4_OVARY	71649944	71651168	71650803	71650803	Missense_Mutation	G	A	p.V1387I
RD_SOFT_TISSUE	71649944	71651168	71650889	71650889	Missense_Mutation	A	T	p.K1415N
SHP77_LUNG	71649944	71651168	71650941	71650941	Missense_Mutation	T	G	p.S1433A
HCT15_LARGE_INTESTINE	71649944	71651168	71650944	71650944	Missense_Mutation	G	T	p.A1434S
OELE_OVARY	71649944	71651168	71651028	71651028	Missense_Mutation	A	G	p.S1462G
KP2_PANCREAS	71649944	71651168	71651092	71651092	Missense_Mutation	A	G	p.Y1483C
C75_LARGE_INTESTINE	71649944	71651168	71651104	71651104	Missense_Mutation	C	G	p.T1487R
HS729_SOFT_TISSUE	71649944	71651168	71651130	71651130	Missense_Mutation	A	G	p.R1496G
LNCAPCLONEFGC_PROSTATE	71653590	71654544	71653598	71653598	Missense_Mutation	A	T	p.L1533F
NCIH2170_LUNG	71653590	71654544	71653641	71653641	Missense_Mutation	A	G	p.I1548V
NCIH1339_LUNG	71653590	71654544	71653704	71653704	Missense_Mutation	C	A	p.L1569I
G361_SKIN	71653590	71654544	71653729	71653729	Missense_Mutation	T	G	p.L1577R
MFE319_ENDOMETRIUM	71653590	71654544	71653893	71653893	Missense_Mutation	A	G	p.M1632V
NCIH1915_LUNG	71653590	71654544	71653913	71653913	Missense_Mutation	T	A	p.N1638K
DIFI_LARGE_INTESTINE	71653590	71654544	71653930	71653930	Missense_Mutation	C	A	p.T1644K
COLO699_LUNG	71653590	71654544	71653956	71653956	Missense_Mutation	G	A	p.D1653N
CHL1_SKIN	71653590	71654544	71653956	71653956	Missense_Mutation	G	A	p.D1653N
HMCB_SKIN	71653590	71654544	71653956	71653956	Missense_Mutation	G	A	p.D1653N
EN_ENDOMETRIUM	71653590	71654544	71654014	71654014	Missense_Mutation	A	T	p.Q1672L
IGROV1_OVARY	71653590	71654544	71654034	71654034	Missense_Mutation	C	T	p.R1679C
DIPG007_CENTRAL_NERVOUS_SYSTEM	71653590	71654544	71654449	71654449	Missense_Mutation	A	G	p.K1817R
HT115_LARGE_INTESTINE	71653590	71654544	71654514	71654514	Missense_Mutation	C	A	p.L1839I
NCIH650_LUNG	71658457	71658558	71658494	71658494	Missense_Mutation	G	T	p.E1896D
SNU175_LARGE_INTESTINE	71658457	71658558	71658540	71658540	Missense_Mutation	G	A	p.A1912T
SARC9371_BONE	71658457	71658558	71658552	71658552	Missense_Mutation	C	T	p.P1916S
SNU81_LARGE_INTESTINE	71591084	71591382	71591334	71591334	Nonsense_Mutation	C	T	p.R557*
VMRCLCD_LUNG	71649944	71651168	71650740	71650740	Nonsense_Mutation	G	T	p.G1366*
ISTMEL1_SKIN	71653590	71654544	71653662	71653662	Nonsense_Mutation	C	T	p.Q1555*
HEC251_ENDOMETRIUM	71658457	71658558	71658495	71658495	Nonsense_Mutation	C	T	p.R1897*

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ZNF638

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
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	BRCA	rs2670753	chr2:71575643	A/T	3.68e-07
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	BRCA	rs2670753	chr2:71575643	A/T	1.91e-05
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	BRCA	rs2670753	chr2:71575643	A/T	1.58e-04
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	LGG	rs2670753	chr2:71575643	A/T	3.22e-03
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	KIRC	rs2670753	chr2:71575643	A/T	4.33e-05
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	KIRC	rs2670753	chr2:71575643	A/T	2.45e-04
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	LUAD	rs2670753	chr2:71575643	A/T	8.54e-04
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	OV	rs2670753	chr2:71575643	A/T	1.00e-03
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	OV	rs2670753	chr2:71575643	A/T	1.03e-03
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	PRAD	rs2670753	chr2:71575643	A/T	2.72e-04
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	PRAD	rs2670753	chr2:71575643	A/T	1.53e-03
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	THCA	rs2670753	chr2:71575643	A/T	1.23e-06
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	THCA	rs2670753	chr2:71575643	A/T	1.40e-06
exon_skip_326406	2	71558911:71558995:71575556:71577401:71582848:71582910	71575556:71577401	ENST00000409544.1	THCA	rs2670753	chr2:71575643	A/T	1.56e-05
exon_skip_326451	2	71654479:71654544:71658456:71658558:71660294:71660413	71658456:71658558	ENST00000493576.2	BRCA	rs11542286	chr2:71658541	C/T	3.64e-04
exon_skip_326451	2	71654479:71654544:71658456:71658558:71660294:71660413	71658456:71658558	ENST00000493576.2	BRCA	rs11542286	chr2:71658541	C/T	2.74e-03
exon_skip_326451	2	71654479:71654544:71658456:71658558:71660294:71660413	71658456:71658558	ENST00000493576.2	THCA	rs11542286	chr2:71658541	C/T	1.12e-06
exon_skip_326451	2	71654479:71654544:71658456:71658558:71660294:71660413	71658456:71658558	ENST00000493576.2	THCA	rs11542286	chr2:71658541	C/T	4.66e-05
exon_skip_326451	2	71654479:71654544:71658456:71658558:71660294:71660413	71658456:71658558	ENST00000493576.2	THCA	rs11542286	chr2:71658541	C/T	9.84e-05
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	BLCA	rs1804020	chr2:71654175	G/A	1.78e-03
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	BLCA	rs1804020	chr2:71654175	G/A	1.78e-03
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	BRCA	rs1804020	chr2:71654175	G/A	5.67e-05
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	BRCA	rs1804020	chr2:71654175	G/A	6.42e-04
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	BRCA	rs60163900	chr2:71654450	A/G	1.16e-03
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	BRCA	rs1804020	chr2:71654175	G/A	5.03e-03
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	LIHC	rs1804020	chr2:71654175	G/A	1.23e-03
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	OV	rs1804020	chr2:71654175	G/A	1.20e-03
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	OV	rs1804020	chr2:71654175	G/A	1.22e-03
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	THCA	rs60163900	chr2:71654450	A/G	8.08e-07
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	THCA	rs60163900	chr2:71654450	A/G	2.51e-05
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	THCA	rs60163900	chr2:71654450	A/G	5.88e-05
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	THCA	rs1804020	chr2:71654175	G/A	3.03e-04
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	THCA	rs1804020	chr2:71654175	G/A	1.94e-03
exon_skip_326437	2	71651779:71651845:71653589:71654544:71655676:71655781	71653589:71654544	ENST00000409544.1,ENST00000264447.4,ENST00000409407.1,ENST00000487638.1,ENST00000483421.3,ENST00000355812.3	THCA	rs1804020	chr2:71654175	G/A	2.29e-03

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ZNF638

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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ZNF638

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RelatedDrugs for ZNF638

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 ZNF638

Diseases associated with this gene. (DisGeNet 4.0)

Gene

Disease ID

Disease name

# pubmeds

Source

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