ExonSkipDB: functional annotation of exon skipping event in human

Gene summary for ERICH1

Gene summary

Gene information	Gene symbol	ERICH1
	Gene ID	157697
	Gene name	glutamate rich 1
	Synonyms	HSPC319
	Cytomap	8p23.3
	Type of gene	protein-coding
	Description	glutamate-rich protein 1
	Modification date	20180519
	UniProtAcc	Q86X53
	Context	PubMed: ERICH1 [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 ERICH1 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 ERICH1

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 ERICH1

Information of exkip skipping event in TCGA.

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENSG00000104714.9	ENST00000519909.1
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENSG00000104714.9	ENST00000523415.1
exon_skip_487960	8	614621:614676:618597:618792:623288:623326	618597:618792	ENSG00000104714.9	ENST00000262109.7
exon_skip_487968	8	618597:618792:623288:624047:642477:642612	623288:624047	ENSG00000104714.9	ENST00000262109.7
exon_skip_487972	8	623864:624047:640897:641096:642477:642612	640897:641096	ENSG00000104714.9	ENST00000524138.1
exon_skip_487974	8	623864:624047:642477:642612:665860:665927	642477:642612	ENSG00000104714.9	ENST00000518277.1,ENST00000262109.7
exon_skip_487978	8	642477:642612:665860:666007:681139:681197	665860:666007	ENSG00000104714.9	ENST00000262109.7

PSI values of skipped exons in TCGA.

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Exon skipping events with PSIs in GTEx for ERICH1

Information of exkip skipping event in GTEx

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENSG00000104714.9	ENST00000519909.1
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENSG00000104714.9	ENST00000523415.1
exon_skip_487960	8	614621:614676:618597:618792:623288:623326	618597:618792	ENSG00000104714.9	ENST00000262109.7
exon_skip_487968	8	618597:618792:623288:624047:642477:642612	623288:624047	ENSG00000104714.9	ENST00000262109.7
exon_skip_487972	8	623864:624047:640897:641096:642477:642612	640897:641096	ENSG00000104714.9	ENST00000524138.1
exon_skip_487974	8	623864:624047:642477:642612:665860:665927	642477:642612	ENSG00000104714.9	ENST00000262109.7,ENST00000518277.1
exon_skip_487978	8	642477:642612:665860:666007:681139:681197	665860:666007	ENSG00000104714.9	ENST00000262109.7

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 ERICH1

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
ENST00000262109	618597	618792	In-frame
ENST00000262109	623288	624047	In-frame
ENST00000262109	642477	642612	In-frame
ENST00000262109	665860	666007	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
ENST00000262109	618597	618792	In-frame
ENST00000262109	623288	624047	In-frame
ENST00000262109	642477	642612	In-frame
ENST00000262109	665860	666007	In-frame

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Infer the effects of exon skipping event on protein functional features for ERICH1

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
ENST00000262109	1830	443	665860	666007	101	247	7	56
ENST00000262109	1830	443	642477	642612	248	382	56	101
ENST00000262109	1830	443	623288	624047	383	1141	101	354
ENST00000262109	1830	443	618597	618792	1142	1336	354	419

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
ENST00000262109	1830	443	665860	666007	101	247	7	56
ENST00000262109	1830	443	642477	642612	248	382	56	101
ENST00000262109	1830	443	623288	624047	383	1141	101	354
ENST00000262109	1830	443	618597	618792	1142	1336	354	419

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
Q86X53	7	56	1	443	Chain	ID=PRO_0000087029;Note=Glutamate-rich protein 1
Q86X53	7	56	12	12	Modified residue	Note=N6-acetyllysine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:19608861;Dbxref=PMID:19608861
Q86X53	56	101	1	443	Chain	ID=PRO_0000087029;Note=Glutamate-rich protein 1
Q86X53	101	354	1	443	Chain	ID=PRO_0000087029;Note=Glutamate-rich protein 1
Q86X53	101	354	193	328	Compositional bias	Note=Glu-rich
Q86X53	101	354	238	238	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244\|PubMed:18669648,ECO:0000244\|PubMed:19690332,ECO:0000244\|PubMed:20068231,ECO:0000244\|PubMed:21406692,ECO:0000244\|PubMed:23186163;Dbxref=PMID:1
Q86X53	101	354	254	254	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244;evidence=ECO:0000244\|PubMed:21406692,ECO:0000244\|PubMed:23186163;Dbxref=PMID:21406692,PMID:23186163
Q86X53	101	354	277	277	Modified residue	Note=Phosphothreonine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:19690332;Dbxref=PMID:19690332
Q86X53	354	419	1	443	Chain	ID=PRO_0000087029;Note=Glutamate-rich protein 1
Q86X53	354	419	365	365	Natural variant	ID=VAR_035915;Note=In a colorectal cancer sample%3B somatic mutation. L->F;Ontology_term=ECO:0000269;evidence=ECO:0000269\|PubMed:16959974;Dbxref=dbSNP:rs774405503,PMID:16959974
Q86X53	354	419	403	403	Natural variant	ID=VAR_050974;Note=R->S;Dbxref=dbSNP:rs1703879

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
Q86X53	7	56	1	443	Chain	ID=PRO_0000087029;Note=Glutamate-rich protein 1
Q86X53	7	56	12	12	Modified residue	Note=N6-acetyllysine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:19608861;Dbxref=PMID:19608861
Q86X53	56	101	1	443	Chain	ID=PRO_0000087029;Note=Glutamate-rich protein 1
Q86X53	101	354	1	443	Chain	ID=PRO_0000087029;Note=Glutamate-rich protein 1
Q86X53	101	354	193	328	Compositional bias	Note=Glu-rich
Q86X53	101	354	238	238	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244\|PubMed:18669648,ECO:0000244\|PubMed:19690332,ECO:0000244\|PubMed:20068231,ECO:0000244\|PubMed:21406692,ECO:0000244\|PubMed:23186163;Dbxref=PMID:1
Q86X53	101	354	254	254	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244;evidence=ECO:0000244\|PubMed:21406692,ECO:0000244\|PubMed:23186163;Dbxref=PMID:21406692,PMID:23186163
Q86X53	101	354	277	277	Modified residue	Note=Phosphothreonine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:19690332;Dbxref=PMID:19690332
Q86X53	354	419	1	443	Chain	ID=PRO_0000087029;Note=Glutamate-rich protein 1
Q86X53	354	419	365	365	Natural variant	ID=VAR_035915;Note=In a colorectal cancer sample%3B somatic mutation. L->F;Ontology_term=ECO:0000269;evidence=ECO:0000269\|PubMed:16959974;Dbxref=dbSNP:rs774405503,PMID:16959974
Q86X53	354	419	403	403	Natural variant	ID=VAR_050974;Note=R->S;Dbxref=dbSNP:rs1703879

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SNVs in the skipped exons for ERICH1

- 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.

- 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
STAD	TCGA-BR-6452-01	exon_skip_487968	623289	624047	623321	623321	Frame_Shift_Del	A	-	p.L344fs
COAD	TCGA-AA-3713-01	exon_skip_487968	623289	624047	623865	623865	Frame_Shift_Del	T	-	p.R163fs
COAD	TCGA-CM-5861-01	exon_skip_487968	623289	624047	623865	623865	Frame_Shift_Del	T	-	p.R163fs
HNSC	TCGA-F7-A624-01	exon_skip_487968	623289	624047	623865	623865	Frame_Shift_Del	T	-	p.R163fs
KIRC	TCGA-B2-3923-01	exon_skip_487968	623289	624047	623705	623706	Frame_Shift_Ins	-	C	p.E216fs
STAD	TCGA-VQ-A8P2-01	exon_skip_487968	623289	624047	623864	623865	Frame_Shift_Ins	-	T	p.E163fs
STAD	TCGA-VQ-A8P2-01	exon_skip_487968	623289	624047	623864	623865	Frame_Shift_Ins	-	T	p.R163fs
COAD	TCGA-AZ-4615-01	exon_skip_487968	623289	624047	623985	623986	Frame_Shift_Ins	-	T	p.F123fs
BLCA	TCGA-ZF-A9R2-01	exon_skip_487968	623289	624047	623493	623493	Nonsense_Mutation	C	A	p.E287*
COAD	TCGA-D5-6928-01	exon_skip_487968	623289	624047	623517	623517	Nonsense_Mutation	C	A	p.E279X
SKCM	TCGA-FW-A5DX-01	exon_skip_487968	623289	624047	623733	623733	Nonsense_Mutation	C	A	p.E207*
SKCM	TCGA-FW-A5DX-01	exon_skip_487968	623289	624047	623733	623733	Nonsense_Mutation	C	A	p.E207X
STAD	TCGA-CD-8536-01	exon_skip_487968	623289	624047	624006	624006	Nonsense_Mutation	T	A	p.K116*
STAD	TCGA-CD-8536-01	exon_skip_487968	623289	624047	624006	624006	Nonsense_Mutation	T	A	p.K116X
TGCT	TCGA-YU-A90W-01	exon_skip_487974	642478	642612	642586	642586	Nonsense_Mutation	G	A	p.R66*
TGCT	TCGA-YU-A90W-01	exon_skip_487974	642478	642612	642586	642586	Nonsense_Mutation	G	A	p.R66X

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

Depth of coverage in three exons

Mutation description

- 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
NCIH1623_LUNG	623289	624047	623734	623738	Frame_Shift_Del	ACAAG	-	p.AC205fs
NCIH1623_LUNG	623289	624047	623740	623741	Frame_Shift_Ins	-	TGGTA	p.E204fs
BCP1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623667	623684	In_Frame_Del	TATCTTTAACGTCTTCCT	-	p.223_229EEDVKDT>A
LCLC97TM1_LUNG	623289	624047	623667	623684	In_Frame_Del	TATCTTTAACGTCTTCCT	-	p.223_229EEDVKDT>A
TALL1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623667	623684	In_Frame_Del	TATCTTTAACGTCTTCCT	-	p.223_229EEDVKDT>A
LCLC97TM1_LUNG	623289	624047	623688	623693	In_Frame_Del	CGGCCA	-	p.220_222LAG>R
TALL1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623688	623693	In_Frame_Del	CGGCCA	-	p.220_222LAG>R
SISO_CERVIX	618598	618792	618697	618697	Missense_Mutation	A	G	p.S387P
GRST_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	618598	618792	618697	618697	Missense_Mutation	A	G	p.S387P
IGROV1_OVARY	618598	618792	618726	618726	Missense_Mutation	G	A	p.A377V
RKO_LARGE_INTESTINE	623289	624047	623453	623453	Missense_Mutation	T	C	p.D300G
MEC1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623460	623460	Missense_Mutation	C	T	p.G298S
MCC13_SKIN	623289	624047	623466	623466	Missense_Mutation	C	T	p.E296K
RAMOS2G64C10_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623474	623474	Missense_Mutation	G	A	p.T293I
NCIH1963_LUNG	623289	624047	623595	623595	Missense_Mutation	C	T	p.A253T
NCIH2141_LUNG	623289	624047	623607	623607	Missense_Mutation	C	T	p.E249K
NCIH748_LUNG	623289	624047	623631	623631	Missense_Mutation	C	A	p.D241Y
MCC13_SKIN	623289	624047	623666	623666	Missense_Mutation	G	A	p.T229I
HEC59_ENDOMETRIUM	623289	624047	623728	623728	Missense_Mutation	C	G	p.E208D
JHOS4_OVARY	623289	624047	623728	623728	Missense_Mutation	C	G	p.E208D
NUGC2_STOMACH	623289	624047	623728	623728	Missense_Mutation	C	G	p.E208D
PL21_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623728	623728	Missense_Mutation	C	G	p.E208D
KMOE2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623728	623728	Missense_Mutation	C	G	p.E208D
SLVL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623728	623728	Missense_Mutation	C	G	p.E208D
HCT15_LARGE_INTESTINE	623289	624047	623740	623740	Missense_Mutation	C	A	p.E204D
SNU1041_UPPER_AERODIGESTIVE_TRACT	623289	624047	623763	623763	Missense_Mutation	T	G	p.N197H
PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623783	623783	Missense_Mutation	T	C	p.Y190C
HEC1_ENDOMETRIUM	623289	624047	623820	623820	Missense_Mutation	C	T	p.G178S
HEC1B_ENDOMETRIUM	623289	624047	623820	623820	Missense_Mutation	C	T	p.G178S
KNS81_CENTRAL_NERVOUS_SYSTEM	623289	624047	623849	623849	Missense_Mutation	T	C	p.K168R
KNS81FD_CENTRAL_NERVOUS_SYSTEM	623289	624047	623849	623849	Missense_Mutation	T	C	p.K168R
D502MG_CENTRAL_NERVOUS_SYSTEM	623289	624047	623873	623873	Missense_Mutation	T	G	p.N160T
NB4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	623289	624047	623976	623976	Missense_Mutation	G	T	p.P126T
HEC251_ENDOMETRIUM	623289	624047	624020	624020	Missense_Mutation	C	A	p.R111I
DMS454_LUNG	623289	624047	624042	624042	Missense_Mutation	C	A	p.D104Y
HT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	642478	642612	642486	642486	Missense_Mutation	T	G	p.D99A
SUPT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	642478	642612	642520	642520	Missense_Mutation	A	C	p.C88G
PCI15A_UPPER_AERODIGESTIVE_TRACT	642478	642612	642555	642555	Missense_Mutation	T	G	p.E76A
HCC2998_LARGE_INTESTINE	642478	642612	642580	642580	Missense_Mutation	G	A	p.L68F
TYKNU_OVARY	665861	666007	665863	665863	Missense_Mutation	G	C	p.T56R
HCC2157_BREAST	665861	666007	666002	666002	Missense_Mutation	C	T	p.V10M
HCC2157_MATCHED_NORMAL_TISSUE	665861	666007	666002	666002	Missense_Mutation	C	T	p.V10M
JHOS4_OVARY	665861	666007	666005	666005	Missense_Mutation	A	C	p.F9V
HMY1_SKIN	665861	666007	666006	666006	Splice_Site	C	G	p.V8V

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ERICH1

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_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	GBM	rs4735891	chr8:576419	G/A	8.35e-10
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	GBM	rs4735891	chr8:576419	G/A	8.35e-10
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	GBM	rs4735890	chr8:576304	A/C	3.08e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	GBM	rs4735890	chr8:576304	A/C	3.08e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	GBM	rs79693921	chr8:575935	C/G	4.01e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	GBM	rs79693921	chr8:575935	C/G	4.01e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	CESC	rs4735891	chr8:576419	G/A	3.42e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	CESC	rs4735891	chr8:576419	G/A	3.42e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	CESC	rs336430	chr8:576209	A/G	4.89e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	CESC	rs336430	chr8:576209	A/G	4.89e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	CESC	rs4735890	chr8:576304	A/C	6.54e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	CESC	rs4735890	chr8:576304	A/C	6.55e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	COAD	rs4735891	chr8:576419	G/A	3.79e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	COAD	rs4735891	chr8:576419	G/A	3.79e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	COAD	rs4735890	chr8:576304	A/C	9.79e-10
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	COAD	rs4735890	chr8:576304	A/C	9.79e-10
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	COAD	rs336430	chr8:576209	A/G	5.09e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	COAD	rs336430	chr8:576209	A/G	5.09e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	BLCA	rs62486186	chr8:576430	G/C	1.40e-10
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	BLCA	rs62486186	chr8:576430	G/C	1.40e-10
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	BLCA	rs336430	chr8:576209	A/G	1.32e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	BLCA	rs336430	chr8:576209	A/G	1.32e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	ESCA	rs79693921	chr8:575935	C/G	1.33e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	ESCA	rs79693921	chr8:575935	C/G	1.33e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	ESCA	rs62486186	chr8:576430	G/C	2.07e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	ESCA	rs62486186	chr8:576430	G/C	2.07e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	ESCA	rs336430	chr8:576209	A/G	5.13e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	ESCA	rs336430	chr8:576209	A/G	5.13e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	HNSC	rs4735891	chr8:576419	G/A	1.06e-18
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	HNSC	rs4735891	chr8:576419	G/A	1.06e-18
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	HNSC	rs4735890	chr8:576304	A/C	1.06e-14
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	HNSC	rs4735890	chr8:576304	A/C	1.06e-14
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	HNSC	rs336430	chr8:576209	A/G	5.22e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	HNSC	rs336430	chr8:576209	A/G	5.22e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	HNSC	rs79693921	chr8:575935	C/G	1.12e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	HNSC	rs79693921	chr8:575935	C/G	1.12e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	BRCA	rs4735890	chr8:576304	A/C	9.57e-20
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	BRCA	rs4735890	chr8:576304	A/C	9.57e-20
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	BRCA	rs336430	chr8:576209	A/G	1.90e-18
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	BRCA	rs336430	chr8:576209	A/G	1.90e-18
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KICH	rs4735891	chr8:576419	G/A	3.68e-09
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KICH	rs4735891	chr8:576419	G/A	3.68e-09
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KICH	rs4735890	chr8:576304	A/C	8.19e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KICH	rs4735890	chr8:576304	A/C	8.19e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs62486186	chr8:576430	G/C	5.77e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs62486186	chr8:576430	G/C	5.77e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs4735891	chr8:576419	G/A	3.16e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs4735891	chr8:576419	G/A	3.16e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs336430	chr8:576209	A/G	6.24e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs336430	chr8:576209	A/G	6.24e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs4735890	chr8:576304	A/C	3.88e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs4735890	chr8:576304	A/C	3.88e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs79693921	chr8:575935	C/G	4.15e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRP	rs79693921	chr8:575935	C/G	4.15e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs4735891	chr8:576419	G/A	3.72e-29
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs4735891	chr8:576419	G/A	3.72e-29
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs4735890	chr8:576304	A/C	7.69e-22
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs4735890	chr8:576304	A/C	7.69e-22
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs62486186	chr8:576430	G/C	3.87e-17
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs62486186	chr8:576430	G/C	3.87e-17
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs336430	chr8:576209	A/G	8.69e-16
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs336430	chr8:576209	A/G	8.69e-16
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs336431	chr8:576324	A/G	3.22e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs336431	chr8:576324	A/G	3.22e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs336432	chr8:576809	T/C	9.55e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LGG	rs336432	chr8:576809	T/C	9.55e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRC	rs4735891	chr8:576419	G/A	2.38e-28
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRC	rs4735891	chr8:576419	G/A	2.38e-28
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRC	rs4735890	chr8:576304	A/C	6.61e-25
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRC	rs4735890	chr8:576304	A/C	6.61e-25
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRC	rs62486186	chr8:576430	G/C	2.76e-23
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRC	rs62486186	chr8:576430	G/C	2.76e-23
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRC	rs336430	chr8:576209	A/G	1.12e-20
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	KIRC	rs336430	chr8:576209	A/G	1.12e-20
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUAD	rs4735891	chr8:576419	G/A	1.16e-18
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUAD	rs4735891	chr8:576419	G/A	1.16e-18
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUAD	rs336430	chr8:576209	A/G	4.16e-16
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUAD	rs336430	chr8:576209	A/G	4.16e-16
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUAD	rs62486186	chr8:576430	G/C	1.39e-15
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUAD	rs62486186	chr8:576430	G/C	1.39e-15
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUAD	rs4735890	chr8:576304	A/C	7.79e-14
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUAD	rs4735890	chr8:576304	A/C	7.79e-14
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	MESO	rs62486186	chr8:576430	G/C	1.18e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	MESO	rs62486186	chr8:576430	G/C	1.18e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	MESO	rs336430	chr8:576209	A/G	1.18e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	MESO	rs336430	chr8:576209	A/G	1.18e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LIHC	rs336430	chr8:576209	A/G	1.83e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LIHC	rs336430	chr8:576209	A/G	1.83e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LIHC	rs4735890	chr8:576304	A/C	6.84e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LIHC	rs4735890	chr8:576304	A/C	6.84e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUSC	rs4735890	chr8:576304	A/C	5.76e-16
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUSC	rs4735890	chr8:576304	A/C	5.78e-16
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUSC	rs4735891	chr8:576419	G/A	8.22e-16
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUSC	rs4735891	chr8:576419	G/A	8.25e-16
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUSC	rs336430	chr8:576209	A/G	4.74e-15
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	LUSC	rs336430	chr8:576209	A/G	4.75e-15
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	OV	rs4735890	chr8:576304	A/C	3.96e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	OV	rs4735890	chr8:576304	A/C	5.48e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	OV	rs336430	chr8:576209	A/G	6.02e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	OV	rs336430	chr8:576209	A/G	1.42e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	READ	rs4735891	chr8:576419	G/A	2.14e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	READ	rs4735891	chr8:576419	G/A	2.14e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	READ	rs4735890	chr8:576304	A/C	5.62e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	READ	rs4735890	chr8:576304	A/C	5.62e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PCPG	rs4735891	chr8:576419	G/A	2.28e-09
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PCPG	rs4735891	chr8:576419	G/A	2.28e-09
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PCPG	rs62486186	chr8:576430	G/C	1.33e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PCPG	rs62486186	chr8:576430	G/C	1.33e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PCPG	rs4735890	chr8:576304	A/C	4.63e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PCPG	rs4735890	chr8:576304	A/C	4.63e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PCPG	rs336430	chr8:576209	A/G	2.99e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PCPG	rs336430	chr8:576209	A/G	2.99e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PAAD	rs4735891	chr8:576419	G/A	1.43e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PAAD	rs4735891	chr8:576419	G/A	1.43e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PAAD	rs4735890	chr8:576304	A/C	3.01e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PAAD	rs4735890	chr8:576304	A/C	3.01e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PAAD	rs336430	chr8:576209	A/G	3.23e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PAAD	rs336430	chr8:576209	A/G	3.23e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PRAD	rs4735891	chr8:576419	G/A	1.50e-15
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PRAD	rs4735891	chr8:576419	G/A	1.50e-15
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PRAD	rs336430	chr8:576209	A/G	1.96e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PRAD	rs336430	chr8:576209	A/G	1.97e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PRAD	rs4735890	chr8:576304	A/C	4.48e-10
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	PRAD	rs4735890	chr8:576304	A/C	4.49e-10
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs4735891	chr8:576419	G/A	2.14e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs4735891	chr8:576419	G/A	2.14e-11
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs4735890	chr8:576304	A/C	9.92e-09
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs4735890	chr8:576304	A/C	9.92e-09
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs336430	chr8:576209	A/G	4.50e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs336430	chr8:576209	A/G	4.50e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs62486186	chr8:576430	G/C	8.26e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs62486186	chr8:576430	G/C	8.26e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs79693921	chr8:575935	C/G	1.10e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	SARC	rs79693921	chr8:575935	C/G	1.10e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THYM	rs62486186	chr8:576430	G/C	1.50e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THYM	rs62486186	chr8:576430	G/C	1.50e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THYM	rs336430	chr8:576209	A/G	5.53e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THYM	rs336430	chr8:576209	A/G	5.53e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THYM	rs79693921	chr8:575935	C/G	9.54e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THYM	rs79693921	chr8:575935	C/G	9.54e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	TGCT	rs62486186	chr8:576430	G/C	7.10e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	TGCT	rs62486186	chr8:576430	G/C	7.10e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	TGCT	rs336430	chr8:576209	A/G	7.40e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	TGCT	rs336430	chr8:576209	A/G	7.40e-08
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs4735891	chr8:576419	G/A	3.33e-12
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs4735891	chr8:576419	G/A	3.33e-12
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs4735890	chr8:576304	A/C	1.58e-09
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs4735890	chr8:576304	A/C	1.58e-09
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs62486186	chr8:576430	G/C	1.98e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs62486186	chr8:576430	G/C	1.98e-07
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs336430	chr8:576209	A/G	2.68e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs336430	chr8:576209	A/G	2.68e-06
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs79693921	chr8:575935	C/G	3.52e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	STAD	rs79693921	chr8:575935	C/G	3.52e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THCA	rs4735891	chr8:576419	G/A	5.62e-29
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THCA	rs4735891	chr8:576419	G/A	5.62e-29
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THCA	rs4735890	chr8:576304	A/C	3.71e-22
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THCA	rs4735890	chr8:576304	A/C	3.71e-22
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THCA	rs62486186	chr8:576430	G/C	8.66e-18
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THCA	rs62486186	chr8:576430	G/C	8.66e-18
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THCA	rs336430	chr8:576209	A/G	2.41e-14
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	THCA	rs336430	chr8:576209	A/G	2.41e-14
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	UVM	rs4735891	chr8:576419	G/A	5.84e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	UVM	rs4735891	chr8:576419	G/A	5.84e-05
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	UCEC	rs336430	chr8:576209	A/G	6.76e-04
exon_skip_487948	8	566525:566581:575674:577238:618597:618792	575674:577238	ENST00000523415.1	UCEC	rs336430	chr8:576209	A/G	6.76e-04
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	GBM	rs79693921	chr8:575935	C/G	4.01e-04
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	GBM	rs79693921	chr8:575935	C/G	4.01e-04
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	ESCA	rs79693921	chr8:575935	C/G	1.33e-05
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	ESCA	rs79693921	chr8:575935	C/G	1.33e-05
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	HNSC	rs79693921	chr8:575935	C/G	1.12e-07
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	HNSC	rs79693921	chr8:575935	C/G	1.12e-07
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	KIRP	rs79693921	chr8:575935	C/G	4.15e-05
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	KIRP	rs79693921	chr8:575935	C/G	4.15e-05
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	SARC	rs79693921	chr8:575935	C/G	1.10e-04
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	SARC	rs79693921	chr8:575935	C/G	1.10e-04
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	THYM	rs79693921	chr8:575935	C/G	9.54e-05
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	THYM	rs79693921	chr8:575935	C/G	9.54e-05
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	STAD	rs79693921	chr8:575935	C/G	3.52e-04
exon_skip_487944	8	566525:566581:575674:575968:577002:577106	575674:575968	ENST00000519909.1	STAD	rs79693921	chr8:575935	C/G	3.52e-04
exon_skip_487978	8	642477:642612:665860:666007:681139:681197	665860:666007	ENST00000262109.7	CESC	rs1869074	chr8:665858	C/T	3.30e-04

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ERICH1

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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ERICH1

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RelatedDrugs for ERICH1

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 ERICH1

Diseases associated with this gene.
(DisGeNet 4.0)

Gene

Disease ID

Disease name

# pubmeds

Source

	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

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Gene summary for ERICH1

Exon skipping events across known transcript of Ensembl for ERICH1 from UCSC genome browser

Gene isoform structures and expression levels for ERICH1

Exon skipping events with PSIs in TCGA for ERICH1

Exon skipping events with PSIs in GTEx for ERICH1

Open reading frame (ORF) annotation in the exon skipping event for ERICH1

Infer the effects of exon skipping event on protein functional features for ERICH1

SNVs in the skipped exons for ERICH1

Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ERICH1

Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ERICH1

Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ERICH1

RelatedDrugs for ERICH1

RelatedDiseases for ERICH1