EuRBPDB

Basic Information
Cancer Related Information

Description

RBPome

Literatures

Expression

Transcripts

Gene Model

Phenotypes

GWAS

PPI

Orthologs

Gene Ontology

Description

Ensembl ID: ENSG00000054523 (Gene tree)
Gene ID: 23095
Gene Symbol: KIF1B
Alias: KIAA0591|KLP|HMSNII|CMT2A|CMT2
Full Name: kinesin family member 1B
Gene Type: protein_coding
Species: Homo_sapiens
Status: confidence
Strand: Plus strand
Length: 170,898 bases
Position: chr1:10,210,706-10,381,603
Accession: 16636
RBP type: non-canonical RBP
Summary: This gene encodes a motor protein that transports mitochondria and synaptic vesicle precursors. Mutations in this gene cause Charcot-Marie-Tooth disease, type 2A1. [provided by RefSeq, Jul 2008]

RNA binding proteome (RBPome)

PID	Title	Method	Time	Author	Doi
30607034	Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)	OOPS & HEK293	2019 Jan 3	Queiroz RML	DOI: 10.1038/s41587-018-0001-2
29431736	Capturing the interactome of newly transcribed RNA	RIC & Hela	2018 Feb 12	Bao X	DOI: 10.1038/nmeth.4595
30352994	Discovery of RNA-binding proteins and characterization of their dynamic responses by enhanced RNA interactome capture	RIC & Jurkat	2018 Oct 23	Perez-Perri JI	DOI:10.1038/s41467-018-06557-8

Literatures on RNA binding capacity

PID	Title	Article	Time	Author	Doi
23342162	Pax6 interactions with chromatin and identification of its novel direct target genes in lens and forebrain.	PLoS One	2013	Xie Q	doi: 10.1371/journal.pone.0054507

Expression

Transcripts

Transcript ID	Name	Length	RefSeq ID	Protein ID	Length	RefSeq ID	UniportKB ID
ENST00000635499	KIF1B-213	2098	-	ENSP00000489057	498 (aa)	-	A0A0U1RQL3
ENST00000465635	KIF1B-206	759	-	-	- (aa)	-	-
ENST00000263934	KIF1B-201	6816	-	ENSP00000263934	1770 (aa)	-	O60333
ENST00000470616	KIF1B-207	519	-	-	- (aa)	-	-
ENST00000483340	KIF1B-208	839	-	-	- (aa)	-	-
ENST00000377086	KIF1B-204	10669	-	ENSP00000366290	1816 (aa)	-	O60333
ENST00000620295	KIF1B-211	8624	-	ENSP00000478500	1809 (aa)	-	Q4R9M9
ENST00000377093	KIF1B-205	7565	-	ENSP00000366297	1153 (aa)	-	O60333
ENST00000377081	KIF1B-202	8746	-	ENSP00000366284	1823 (aa)	-	O60333
ENST00000377083	KIF1B-203	5885	-	ENSP00000366287	1153 (aa)	-	O60333
ENST00000622724	KIF1B-212	8588	-	ENSP00000480063	1797 (aa)	-	A0A087WWA3
ENST00000495136	KIF1B-209	643	-	-	- (aa)	-	-
ENST00000497835	KIF1B-210	452	-	-	- (aa)	-	-

Gene Model

Click here to download ENSG00000054523's gene model file

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000054523	Body Mass Index	5.25291450257361E-6	17903300
ENSG00000054523	Insulin	6.42191882421044E-6	17903298
ENSG00000054523	Glucosephosphate Dehydrogenase	2.781e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	1.4e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	1.016e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	6.866e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	3.522e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	2.781e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	1.15e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	3.873e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	3.873e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	1.4e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	2.781e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	1.4e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	1.15e-005	-
ENSG00000054523	Glucosephosphate Dehydrogenase	1.4e-005	-
ENSG00000054523	Multiple Sclerosis	3E-10	18997785
ENSG00000054523	Carcinoma, Hepatocellular	2E-18	20676096
ENSG00000054523	Cerebrospinal Fluid	4E-10	28031287
ENSG00000054523	Mean Platelet Volume	3E-8	22139419

GWAS

ensgID	SNP	Chromosome	Position	SNP-risk	Trait	PubmedID	95% CI	Or or BEAT	EFO ID
ENSG00000054523	rs17401966	1	10325413	G	Hepatitis B virus-related hepatocellular carcinoma	29246937	[1.43-2.44]	1.89	EFO_0000182\|EFO_0004197
ENSG00000054523	rs11121529	1	10211630	G	Mean platelet volume	27863252	[0.067-0.089] unit increase	0.07830624	EFO_0004584
ENSG00000054523	rs17034775	1	10338950	?	Virologic severity in Herpes simplex virus type 2 infection	29535370			EFO_0009010
ENSG00000054523	rs17034615	1	10251819	?	Cerebrospinal fluid biomarker levels	28031287			EFO_0006794
ENSG00000054523	rs17396340	1	10226118	A	Mean platelet volume	22139419	[0.0041-0.0119] ln(fl) increase	0.008	EFO_0004584
ENSG00000054523	rs12137527	1	10255239	?	Tonsillectomy	28928442	[0.038-0.085] unit decrease	0.0617	EFO_0007924
ENSG00000054523	rs12141192	1	10371074	?	Tonsillectomy	28928442	[0.035-0.082] unit increase	0.0589	EFO_0007924
ENSG00000054523	rs112682076	1	10297748	C	Hematocrit	27863252	[0.065-0.132] unit decrease	0.09869539	EFO_0004348
ENSG00000054523	rs17401966	1	10325413	A	Hepatocellular carcinoma	20676096	[1.49-1.82]	1.64	EFO_0000182
ENSG00000054523	rs10492972	1	10293054	C	Multiple sclerosis	18997785	[1.23-1.48]	1.34	EFO_0003885
ENSG00000054523	rs17396340	1	10226118	A	Waist circumference adjusted for BMI (adjusted for smoking behaviour)	28443625	[0.019-0.035] unit increase	0.027	EFO_0004318\|EFO_0007789
ENSG00000054523	rs17396340	1	10226118	A	Waist circumference adjusted for BMI (joint analysis main effects and smoking interaction)	28443625			EFO_0004318\|EFO_0007789
ENSG00000054523	rs17396340	1	10226118	A	Waist circumference adjusted for BMI in non-smokers	28443625	[0.024-0.04] unit increase	0.032	EFO_0007789
ENSG00000054523	rs11121542	1	10333862	A	Hand grip strength	29691431	[0.0022-0.0038] unit decrease	0.003	EFO_0006941
ENSG00000054523	rs151178549	1	10252387	?	Heel bone mineral density	30048462	[0.0096-0.0186] unit increase	0.0140716	EFO_0009270
ENSG00000054523	rs111368727	1	10283239	?	Heel bone mineral density	30048462	[0.013-0.024] unit increase	0.0182041	EFO_0009270
ENSG00000054523	rs112682076	1	10297748	?	White blood cell count	30595370			EFO_0004308
ENSG00000054523	rs4846204	1	10248900	?	Red blood cell count	30595370			EFO_0004305
ENSG00000054523	rs112682076	1	10297748	?	Lung function (FEV1/FVC)	30595370			EFO_0004713
ENSG00000054523	rs4846204	1	10248900	T	Body fat distribution (leg fat ratio)	30664634	NR unit decrease (replication)	0.02362	EFO_0004341
ENSG00000054523	rs4846204	1	10248900	T	Body fat distribution (leg fat ratio)	30664634	NR unit decrease (replication)	0.02134	EFO_0004341
ENSG00000054523	rs4846204	1	10248900	T	Body fat distribution (trunk fat ratio)	30664634	NR unit increase (replication)	0.02471	EFO_0004341
ENSG00000054523	rs4846204	1	10248900	T	Body fat distribution (trunk fat ratio)	30664634	NR unit increase (replication)	0.02672	EFO_0004341
ENSG00000054523	rs4846204	1	10248900	T	Body fat distribution (trunk fat ratio)	30664634	NR unit increase (replication)	0.02575	EFO_0004341
ENSG00000054523	rs4846204	1	10248900	T	Body fat distribution (leg fat ratio)	30664634	NR unit decrease (replication)	0.01935	EFO_0004341

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000054523's network

* RBP PPI network refers to all genes directly bind to RBP

Orthologs identified by RBPome

Ensembl ID	Gene Symbol	Coverage	Identiy	Ortholog	Gene Symbol	Coverage	Identiy	Species
ENSG00000054523	KIF1B	100	97.062	ENSMUSG00000063077	Kif1b	100	97.062	Mus_musculus

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0003777	microtubule motor activity	21873635.	IBA	Function
GO:0003777	microtubule motor activity	-	ISS	Function
GO:0005515	protein binding	16225668.20852589.25416956.	IPI	Function
GO:0005524	ATP binding	-	IEA	Function
GO:0005739	mitochondrion	-	IEA	Component
GO:0005871	kinesin complex	21873635.	IBA	Component
GO:0005874	microtubule	21873635.	IBA	Component
GO:0005875	microtubule associated complex	-	ISS	Component
GO:0006915	apoptotic process	-	IEA	Process
GO:0007018	microtubule-based movement	21873635.	IBA	Process
GO:0007018	microtubule-based movement	-	ISS	Process
GO:0007270	neuron-neuron synaptic transmission	-	ISS	Process
GO:0007274	neuromuscular synaptic transmission	-	ISS	Process
GO:0008017	microtubule binding	21873635.	IBA	Function
GO:0008089	anterograde axonal transport	-	ISS	Process
GO:0008574	ATP-dependent microtubule motor activity, plus-end-directed	21873635.	IBA	Function
GO:0010628	positive regulation of gene expression	-	IEA	Process
GO:0016192	vesicle-mediated transport	21873635.	IBA	Process
GO:0016887	ATPase activity	21873635.	IBA	Function
GO:0016887	ATPase activity	-	ISS	Function
GO:0019894	kinesin binding	10341097.	TAS	Function
GO:0019900	kinase binding	-	IEA	Function
GO:0030424	axon	21873635.	IBA	Component
GO:0030425	dendrite	21873635.	IBA	Component
GO:0030659	cytoplasmic vesicle membrane	-	ISS	Component
GO:0030705	cytoskeleton-dependent intracellular transport	21873635.	IBA	Process
GO:0030705	cytoskeleton-dependent intracellular transport	-	ISS	Process
GO:0031410	cytoplasmic vesicle	21873635.	IBA	Component
GO:0031410	cytoplasmic vesicle	-	ISS	Component
GO:0032418	lysosome localization	-	IEA	Process
GO:0043005	neuron projection	21873635.	IBA	Component
GO:0043005	neuron projection	-	ISS	Component
GO:0047497	mitochondrion transport along microtubule	-	IEA	Process
GO:0097110	scaffold protein binding	-	IEA	Function
GO:1904115	axon cytoplasm	-	IEA	Component
GO:1904647	response to rotenone	-	IEA	Process
GO:1990048	anterograde neuronal dense core vesicle transport	-	IEA	Process
GO:1990049	retrograde neuronal dense core vesicle transport	-	IEA	Process
GO:1990090	cellular response to nerve growth factor stimulus	-	IEA	Process
GO:1990778	protein localization to cell periphery	-	IEA	Process

Cancer associated literatures

PID	Title	Article	Time	Author	Doi
24469107	RNA helicase A is a downstream mediator of KIF1Bβ tumor-suppressor function in neuroblastoma.	Cancer Discov	2014 Apr	Chen ZX	doi: 10.1158/2159-8290.CD-13-0362
25518808	The tumour suppressor DLC2 ensures mitotic fidelity by coordinating spindle positioning and cell-cell adhesion.	Nat Commun	2014 Dec 18	Vitiello E	doi: 10.1038/ncomms6826.
18614535	KIF1Bbeta functions as a haploinsufficient tumor suppressor gene mapped to chromosome 1p36.2 by inducing apoptotic cell death.	J Biol Chem	2008 Sep 5	Munirajan AK	doi: 10.1074/jbc.M802316200
12888911	Genomic structure and mutational analysis of the human KIF1Balpha gene located at 1p36.2 in neuroblastoma.	Int J Oncol	2003 Sep	Chen YY	-
25854172	Polymorphisms in the kinesin-like factor 1 B gene and risk of epithelial ovarian cancer in Eastern Chinese women.	Tumour Biol	2015 Sep	Shi TY	doi: 10.1007/s13277-015-3394-2

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
ACC	chr1	10304566	Intron	novel		0.48
BLCA	chr1	10295127	Silent	novel	S544S	0.51
BLCA	chr1	10304517	Intron	novel		0.29
BLCA	chr1	10376649	3'UTR	novel		0.36
BLCA	chr1	10296998	Missense_Mutation	novel	E655K	0.13
BLCA	chr1	10304607	Intron	novel		0.39
BLCA	chr1	10326281	Missense_Mutation	rs141942131	T949M	0.33
BLCA	chr1	10304038	Intron	novel		0.62
BLCA	chr1	10360966	Silent	novel	L1365L	0.1
BLCA	chr1	10371228	Silent	novel	L1638L	0.12
BLCA	chr1	10321706	Splice_Region	novel		0.28
BLCA	chr1	10258522	Missense_Mutation	rs765503412	N71K	0.1
BLCA	chr1	10304240	Intron	novel		0.11
BLCA	chr1	10304038	Intron	novel		0.51
BLCA	chr1	10304607	Intron	novel		0.38
BLCA	chr1	10275449	Missense_Mutation	novel	D302H	0.31
BLCA	chr1	10374422	Missense_Mutation	rs764494187	E1685K	0.45
BLCA	chr1	10321848	Silent	novel	L783L	0.2
BLCA	chr1	10295156	Missense_Mutation	novel	G554E	0.12
BLCA	chr1	10376674	3'UTR	novel		0.45
BLCA	chr1	10337402	Missense_Mutation	novel	K1097N	0.16
BLCA	chr1	10365439	Missense_Mutation	rs774445070	R1515C	0.27
BLCA	chr1	10324881	Missense_Mutation	novel	F887L	0.24
BLCA	chr1	10232413	Nonsense_Mutation	NA	Q29*	0.23
BLCA	chr1	10303586	Intron	novel		0.26
BLCA	chr1	10321706	Splice_Region	novel		0.24
BLCA	chr1	10320049	Nonsense_Mutation	novel	E708*	0.29
BLCA	chr1	10304650	Intron	novel		0.38
BLCA	chr1	10304144	Intron	novel		0.38
BLCA	chr1	10304468	Intron	rs757702990		0.1
BLCA	chr1	10282533	Splice_Region	NA	K478K	0.32
BLCA	chr1	10296968	Missense_Mutation	novel	E645Q	0.18
BLCA	chr1	10275427	Splice_Site	NA	X295_splice	0.14
BLCA	chr1	10303540	Intron	novel		0.22
BLCA	chr1	10258517	Missense_Mutation	novel	Q70E	0.08
BLCA	chr1	10268258	Missense_Mutation	novel	E239K	0.31
BLCA	chr1	10336667	Missense_Mutation	novel	E1018D	0.24
BLCA	chr1	10303702	Intron	novel		0.07
BRCA	chr1	10303741	Intron	novel		0.36
BRCA	chr1	10304009	Intron	rs542546734		0.38
BRCA	chr1	10258495	Splice_Region	novel	P62P	0.22
BRCA	chr1	10352730	Missense_Mutation	NA	S1350C	0.48
BRCA	chr1	10295696	Silent	NA	I569I	0.2
BRCA	chr1	10272258	Silent	NA	N272N	0.16
BRCA	chr1	10304321	Intron	novel		0.04
BRCA	chr1	10337179	Missense_Mutation	novel	E1079Q	0.1
BRCA	chr1	10337122	Missense_Mutation	NA	E1060K	0.82
BRCA	chr1	10324891	Missense_Mutation	novel	G891R	0.05
BRCA	chr1	10303756	Intron	NA		0.17
BRCA	chr1	10295083	Splice_Region	novel		0.78
BRCA	chr1	10352639	Missense_Mutation	rs764473301	R1320W	0.57
BRCA	chr1	10360945	Missense_Mutation	NA	E1358Q	0.31
BRCA	chr1	10378247	3'UTR	novel		0.27
BRCA	chr1	10303783	Intron	NA		0.41
BRCA	chr1	10365582	Missense_Mutation	NA	E1562D	0.23
BRCA	chr1	10296653	Missense_Mutation	NA	Q617E	0.33
BRCA	chr1	10278021	Missense_Mutation	NA	A358V	0.11
BRCA	chr1	10326196	Missense_Mutation	NA	T921A	0.89
BRCA	chr1	10352639	Missense_Mutation	rs764473301	R1320W	0.42
BRCA	chr1	10352639	Missense_Mutation	rs764473301	R1320W	0.27
BRCA	chr1	10258515	Missense_Mutation	NA	S69F	0.24
BRCA	chr1	10304051	Intron	rs377168351		0.17
CESC	chr1	10324789	Missense_Mutation	NA	D857H	0.27
CESC	chr1	10267394	Missense_Mutation	NA	E148D	0.19
CESC	chr1	10275427	Splice_Site	novel	X295_splice	0.46
CESC	chr1	10379089	3'UTR	novel		0.4
CESC	chr1	10365151	Missense_Mutation	NA	R1473Q	0.62
CESC	chr1	10303361	Intron	NA		0.44
CESC	chr1	10365498	Silent	NA	L1534L	0.4
CESC	chr1	10365599	Missense_Mutation	NA	S1568L	0.45
CESC	chr1	10268240	Missense_Mutation	NA	E233K	0.18
CESC	chr1	10371164	Silent	novel	G1616G	0.35
CESC	chr1	10339807	Missense_Mutation	NA	P1154L	0.37
CESC	chr1	10326175	Missense_Mutation	novel	S914P	0.07
CESC	chr1	10303765	Intron	rs755578632		0.32
CESC	chr1	10381264	3'UTR	novel		0.4
CESC	chr1	10279118	Missense_Mutation	novel	Y401F	0.24
CESC	chr1	10361022	Missense_Mutation	NA	M1383I	0.14
CESC	chr1	10324895	Missense_Mutation	NA	S892I	0.37
CESC	chr1	10267414	Missense_Mutation	rs752393884	R155Q	0.31
CHOL	chr1	10374934	Missense_Mutation	rs778439251	R1726H	0.5
COAD	chr1	10376569	Silent	rs768290105	P1811P	0.26
COAD	chr1	10261960	Missense_Mutation	NA	Y140C	0.28
COAD	chr1	10363292	Silent	NA	V1438V	0.34
COAD	chr1	10352649	Missense_Mutation	NA	P1323H	0.17
COAD	chr1	10326126	Silent	rs566526002	H897H	0.07
COAD	chr1	10304051	Intron	rs377168351		0.37
COAD	chr1	10303187	Intron	novel		0.17
COAD	chr1	10304278	Intron	NA		0.37
COAD	chr1	10258629	Missense_Mutation	novel	M107T	0.34
COAD	chr1	10378423	3'UTR	novel		0.21
COAD	chr1	10296659	Missense_Mutation	rs752648536	R619C	0.25
COAD	chr1	10334587	Missense_Mutation	novel	E998Q	0.31
COAD	chr1	10375031	Silent	novel	Q1758Q	0.17
COAD	chr1	10361776	Missense_Mutation	rs143800192	R1419C	0.2
COAD	chr1	10374349	Silent	NA	P1660P	0.29
COAD	chr1	10368523	Silent	rs749686737	S1603S	0.23
COAD	chr1	10304456	Intron	NA		0.41
COAD	chr1	10297003	Silent	NA	P656P	0.13
COAD	chr1	10374407	Nonsense_Mutation	novel	R1680*	0.32
COAD	chr1	10378613	3'UTR	novel		0.26
COAD	chr1	10282476	Silent	NA	S459S	0.26
COAD	chr1	10326321	Silent	rs763515223	P962P	0.06
COAD	chr1	10296993	Missense_Mutation	novel	P653R	0.23
COAD	chr1	10378438	3'UTR	novel		0.29
COAD	chr1	10361031	Silent	rs116302604	S1386S	0.27
COAD	chr1	10279111	Missense_Mutation	novel	D399N	0.16
COAD	chr1	10371165	Missense_Mutation	rs765259892	R1617W	0.15
COAD	chr1	10297028	Missense_Mutation	NA	E665K	0.37
COAD	chr1	10337438	Silent	NA	N1109N	0.43
COAD	chr1	10282333	Missense_Mutation	novel	F412V	0.18
COAD	chr1	10297072	Missense_Mutation	NA	E679D	0.22
COAD	chr1	10324847	Missense_Mutation	NA	G876D	0.26
COAD	chr1	10258615	Silent	NA	G102G	0.35
COAD	chr1	10296903	Missense_Mutation	NA	R623H	0.33
COAD	chr1	10303874	Intron	NA		0.25
COAD	chr1	10378002	3'UTR	novel		0.5
COAD	chr1	10375033	Missense_Mutation	novel	Q1759R	0.06
COAD	chr1	10304819	Intron	novel		0.19
COAD	chr1	10278037	Frame_Shift_Del	novel	*N365Mfs8**	0.32
COAD	chr1	10278052	Silent	NA	L368L	0.18
COAD	chr1	10368524	Missense_Mutation	rs769092155	V1604I	0.21
COAD	chr1	10324868	Missense_Mutation	NA	R883Q	0.29
COAD	chr1	10376577	Missense_Mutation	rs761319935	S1814L	0.33
COAD	chr1	10304165	Intron	rs758844384		0.22
COAD	chr1	10363305	Missense_Mutation	NA	E1443K	0.2
COAD	chr1	10267454	Silent	NA	V168V	0.33
COAD	chr1	10304456	Intron	NA		0.31
COAD	chr1	10323990	Missense_Mutation	rs766572494	R822H	0.29
COAD	chr1	10258635	Missense_Mutation	NA	G109V	0.41
ESCA	chr1	10304433	Intron	novel		0.39
ESCA	chr1	10374342	Missense_Mutation	novel	S1658C	0.33
ESCA	chr1	10337465	Silent	novel	T1118T	0.18
ESCA	chr1	10379135	3'UTR	novel		0.68
GBM	chr1	10326293	Nonsense_Mutation	novel	S953*	0.04
GBM	chr1	10365440	Missense_Mutation	rs375130478	R1515H	0.45
GBM	chr1	10374355	Silent	novel	P1662P	0.13
GBM	chr1	10326297	Missense_Mutation	novel	D954E	0.08
GBM	chr1	10324054	Missense_Mutation	novel	E843D	0.2
GBM	chr1	10361010	Missense_Mutation	novel	E1379D	0.23
GBM	chr1	10365482	Missense_Mutation	rs781051649	S1529L	0.22
GBM	chr1	10374955	Missense_Mutation	novel	Y1733S	0.45
GBM	chr1	10276364	Silent	rs771891729	A334A	0.67
GBM	chr1	10361713	Missense_Mutation	novel	A1398S	0.12
GBM	chr1	10278091	Silent	novel	D381D	0.06
GBM	chr1	10324867	Missense_Mutation	novel	R883W	0.41
GBM	chr1	10324759	Nonsense_Mutation	novel	Q847*	0.19
GBM	chr1	10376551	Silent	novel	K1805K	0.18
GBM	chr1	10337521	Missense_Mutation	novel	F1137S	0.04
HNSC	chr1	10304262	Intron	novel		0.05
HNSC	chr1	10326310	Missense_Mutation	novel	G959W	0.25
HNSC	chr1	10324778	Missense_Mutation	rs752039135	R853Q	0.28
HNSC	chr1	10258568	Missense_Mutation	rs561371619	E87Q	0.3
HNSC	chr1	10295106	Silent	novel	L537L	0.28
HNSC	chr1	10304119	Intron	novel		0.44
HNSC	chr1	10304097	Intron	novel		0.21
HNSC	chr1	10365538	Missense_Mutation	novel	Q1548E	0.23
HNSC	chr1	10296601	Silent	novel	P599P	0.49
HNSC	chr1	10337498	Silent	novel	I1129I	0.3
HNSC	chr1	10334576	Missense_Mutation	novel	A994V	0.27
HNSC	chr1	10365406	Splice_Region	novel		0.21
HNSC	chr1	10297226	Missense_Mutation	novel	L699I	0.11
HNSC	chr1	10374430	Silent	novel	L1687L	0.36
HNSC	chr1	10268188	Silent	novel	S215S	0.42
KICH	chr1	10304589	Intron	novel		0.43
KIRC	chr1	10374436	Silent	novel	L1689L	0.25
KIRC	chr1	10324007	Missense_Mutation	NA	E828K	0.05
KIRC	chr1	10303823	Intron	NA		0.19
KIRC	chr1	10361714	Missense_Mutation	NA	A1398V	0.34
KIRC	chr1	10304510	Intron	NA		0.24
KIRC	chr1	10334581	Missense_Mutation	rs145596547	V996I	0.33
KIRC	chr1	10374464	Missense_Mutation	rs757564628	S1699R	0.35
KIRC	chr1	10352660	Missense_Mutation	NA	E1327K	0.35
KIRC	chr1	10282385	Missense_Mutation	novel	G429A	0.26
KIRC	chr1	10304486	Intron	novel		0.45
KIRC	chr1	10365601	Missense_Mutation	NA	G1569R	0.35
KIRP	chr1	10278051	Missense_Mutation	novel	L368Q	0.47
KIRP	chr1	10282435	Missense_Mutation	NA	C446S	0.15
KIRP	chr1	10278068	Nonsense_Mutation	novel	E374*	0.36
KIRP	chr1	10360928	Splice_Site	novel	X1352_splice	0.06
KIRP	chr1	10304400	Intron	novel		0.28
KIRP	chr1	10268252	Missense_Mutation	NA	S237P	0.24
KIRP	chr1	10232381	Missense_Mutation	novel	R18L	0.06
KIRP	chr1	10334547	Silent	novel	L984L	0.41
LAML	chr1	10275481	Silent	novel	T312T	0.04
LGG	chr1	10326300	Silent	rs771415270	L955L	0.8
LGG	chr1	10326179	Missense_Mutation	rs749523745	T915M	0.07
LGG	chr1	10304137	Intron	novel		0.06
LGG	chr1	10376559	Missense_Mutation	rs770215708	R1808H	0.35
LIHC	chr1	10321855	Missense_Mutation	NA	K786Q	0.24
LIHC	chr1	10256297	Missense_Mutation	novel	D53N	0.14
LIHC	chr1	10324843	Missense_Mutation	novel	T875P	0.44
LIHC	chr1	10352685	Missense_Mutation	novel	S1335F	0.7
LIHC	chr1	10348684	Missense_Mutation	novel	H1300Q	0.32
LIHC	chr1	10348664	Missense_Mutation	NA	I1294F	0.31
LUAD	chr1	10334599	Missense_Mutation	NA	V1002M	0.27
LUAD	chr1	10276397	Splice_Region	novel	L345L	0.1
LUAD	chr1	10304596	Intron	novel		0.19
LUAD	chr1	10275432	Missense_Mutation	novel	K296I	0.04
LUAD	chr1	10282326	Silent	NA	L409L	0.13
LUAD	chr1	10365498	Silent	NA	L1534L	0.3
LUAD	chr1	10267502	Silent	NA	L184L	0.48
LUAD	chr1	10304252	Intron	novel		0.19
LUAD	chr1	10321716	Missense_Mutation	NA	W739C	0.08
LUAD	chr1	10232416	Missense_Mutation	NA	M30V	0.47
LUAD	chr1	10282363	Missense_Mutation	NA	A422P	0.06
LUAD	chr1	10267457	Silent	novel	R169R	0.32
LUAD	chr1	10303937	Intron	novel		0.16
LUAD	chr1	10375307	Missense_Mutation	novel	A1781V	0.28
LUAD	chr1	10304031	Intron	novel		0.4
LUAD	chr1	10326109	Splice_Site	novel	X892_splice	0.21
LUAD	chr1	10361782	Missense_Mutation	NA	L1421V	0.06
LUAD	chr1	10304276	Intron	novel		0.26
LUAD	chr1	10295680	Missense_Mutation	novel	E564V	0.14
LUAD	chr1	10303817	Intron	novel		0.21
LUAD	chr1	10326262	Missense_Mutation	rs142567076	A943T	0.49
LUAD	chr1	10363283	Splice_Region	NA	S1435S	0.25
LUAD	chr1	10375043	Silent	novel	V1762V	0.62
LUAD	chr1	10323883	Splice_Site	novel	X787_splice	0.19
LUAD	chr1	10323979	Missense_Mutation	NA	R818S	0.29
LUAD	chr1	10337119	Missense_Mutation	novel	E1059K	0.2
LUAD	chr1	10295706	Missense_Mutation	NA	G573W	0.18
LUAD	chr1	10371168	Missense_Mutation	NA	D1618Y	0.44
LUAD	chr1	10278046	Silent	novel	A366A	0.26
LUAD	chr1	10347827	Splice_Region	NA	Q1288Q	0.22
LUAD	chr1	10304607	Intron	novel		0.21
LUAD	chr1	10295126	Frame_Shift_Ins	novel	E545*	0.07
LUAD	chr1	10376572	Missense_Mutation	NA	S1812R	0.55
LUSC	chr1	10278071	Nonsense_Mutation	novel	E375*	0.17
LUSC	chr1	10337493	Nonsense_Mutation	novel	G1128*	0.19
LUSC	chr1	10296666	Splice_Site	novel	X621_splice	0.54
LUSC	chr1	10303454	Intron	novel		0.07
LUSC	chr1	10334581	Missense_Mutation	rs145596547	V996I	0.17
LUSC	chr1	10374449	Missense_Mutation	NA	E1694Q	0.05
LUSC	chr1	10268165	Missense_Mutation	NA	T208A	0.17
LUSC	chr1	10296660	Missense_Mutation	rs202061430	R619H	0.3
LUSC	chr1	10268244	Missense_Mutation	NA	T234N	0.55
LUSC	chr1	10374937	Missense_Mutation	NA	R1727L	0.07
LUSC	chr1	10232349	Silent	novel	K7K	0.41
LUSC	chr1	10303893	Intron	rs754969112		0.13
LUSC	chr1	10326189	Silent	rs774630480	S918S	0.18
LUSC	chr1	10365559	Missense_Mutation	NA	E1555K	0.07
LUSC	chr1	10371238	Missense_Mutation	NA	S1641C	0.05
LUSC	chr1	10295102	Missense_Mutation	novel	N536I	0.22
LUSC	chr1	10304565	Intron	rs776976329		0.46
LUSC	chr1	10365104	Missense_Mutation	NA	M1457I	0.43
LUSC	chr1	10282496	Missense_Mutation	NA	S466C	0.26
LUSC	chr1	10320089	Missense_Mutation	rs763303622	R721Q	0.23
LUSC	chr1	10276350	Missense_Mutation	NA	A330S	0.19
LUSC	chr1	10365595	Missense_Mutation	NA	D1567N	0.46
LUSC	chr1	10304038	Intron	novel		0.29
LUSC	chr1	10323985	Silent	rs751285467	F820F	0.44
LUSC	chr1	10267446	Missense_Mutation	novel	L166V	0.33
LUSC	chr1	10278113	Nonsense_Mutation	novel	G389*	0.36
LUSC	chr1	10304228	Intron	novel		0.27
LUSC	chr1	10343279	Missense_Mutation	NA	S1227Y	0.82
LUSC	chr1	10363287	Nonsense_Mutation	novel	R1437*	0.14
LUSC	chr1	10345912	Silent	NA	L1252L	0.49
LUSC	chr1	10276364	Silent	NA	A334A	0.44
LUSC	chr1	10326253	Missense_Mutation	rs764144206	V940M	0.07
LUSC	chr1	10365107	Silent	NA	Q1458Q	0.31
LUSC	chr1	10303347	Intron	novel		0.44
LUSC	chr1	10303300	Intron	novel		0.21
LUSC	chr1	10268190	Missense_Mutation	novel	R216H	0.11
OV	chr1	10323974	Missense_Mutation	novel	D817N	0.04
OV	chr1	10376747	3'UTR	novel		0.16
OV	chr1	10295693	Silent	novel	D568D	0.36
OV	chr1	10295165	Missense_Mutation	novel	R557M	0.34
OV	chr1	10343251	Nonsense_Mutation	NA	R1218*	0.39
OV	chr1	10326307	Missense_Mutation	novel	D958N	0.09
OV	chr1	10365247	Splice_Site	NA	X1504_splice	0.3
OV	chr1	10337149	Nonsense_Mutation	novel	Q1069*	0.04
OV	chr1	10297061	Missense_Mutation	NA	Q676E	0.21
OV	chr1	10375024	Nonsense_Mutation	novel	*E1756delinsDHRIGLGLSV**	0.04
PAAD	chr1	10365442	Missense_Mutation	novel	E1516K	0.18
PAAD	chr1	10326262	Missense_Mutation	rs142567076	A943T	0.2
PAAD	chr1	10352676	Missense_Mutation	novel	A1332V	0.18
PRAD	chr1	10304507	Intron	novel		0.53
PRAD	chr1	10304509	Intron	novel		0.56
PRAD	chr1	10232424	Silent	NA	G32G	0.15
PRAD	chr1	10320060	Silent	NA	L711L	0.21
PRAD	chr1	10303419	Intron	NA		0.08
READ	chr1	10304209	Intron	novel		0.16
READ	chr1	10258659	Missense_Mutation	NA	G117D	0.32
READ	chr1	10323990	Missense_Mutation	rs766572494	R822H	0.08
READ	chr1	10365609	Silent	rs750386624	I1571I	0.43
READ	chr1	10258535	Missense_Mutation	novel	D76Y	0.38
READ	chr1	10304164	Intron	rs752757940		0.44
READ	chr1	10378352	3'UTR	novel		0.39
READ	chr1	10296903	Missense_Mutation	NA	R623H	0.13
READ	chr1	10304362	Intron	NA		0.38
SARC	chr1	10323935	Missense_Mutation	NA	P804S	0.26
SARC	chr1	10363344	Missense_Mutation	novel	G1456S	0.18
SARC	chr1	10380820	3'UTR	novel		0.31
SARC	chr1	10343249	Missense_Mutation	novel	R1217H	0.18
SARC	chr1	10258580	Missense_Mutation	novel	V91F	0.21
SARC	chr1	10376750	3'UTR	novel		0.32
SKCM	chr1	10272275	Missense_Mutation	NA	L278W	0.05
SKCM	chr1	10303940	Intron	novel		0.42
SKCM	chr1	10375344	Silent	NA	A1793A	0.3
SKCM	chr1	10296586	Silent	rs774839409	I594I	0.29
SKCM	chr1	10275458	Missense_Mutation	NA	P305S	0.34
SKCM	chr1	10256267	Missense_Mutation	NA	P43S	0.42
SKCM	chr1	10376749	3'UTR	novel		0.33
SKCM	chr1	10303501	Intron	novel		0.34
SKCM	chr1	10365482	Missense_Mutation	rs781051649	S1529L	0.08
SKCM	chr1	10321816	Silent	NA	L773L	0.32
SKCM	chr1	10374380	Missense_Mutation	novel	P1671S	0.34
SKCM	chr1	10326320	Missense_Mutation	rs762619916	P962L	0.89
SKCM	chr1	10303967	Intron	NA		0.78
SKCM	chr1	10304320	Intron	novel		0.39
SKCM	chr1	10343239	Nonsense_Mutation	NA	Q1214*	0.28
SKCM	chr1	10374440	Missense_Mutation	novel	P1691S	0.28
SKCM	chr1	10337084	Missense_Mutation	rs267597898	S1047L	0.24
SKCM	chr1	10323935	Missense_Mutation	NA	P804S	0.52
SKCM	chr1	10295724	Missense_Mutation	novel	E579K	0.32
SKCM	chr1	10348702	Silent	novel	L1306L	0.59
SKCM	chr1	10334604	Silent	NA	R1003R	0.44
SKCM	chr1	10304097	Intron	novel		0.15
SKCM	chr1	10326264	Silent	rs745644299	A943A	0.57
SKCM	chr1	10365634	Missense_Mutation	NA	E1580K	0.23
SKCM	chr1	10352721	Missense_Mutation	NA	S1347F	0.24
SKCM	chr1	10339811	Silent	NA	L1155L	0.23
SKCM	chr1	10304038	Intron	novel		0.14
SKCM	chr1	10297226	Missense_Mutation	NA	L699F	0.98
SKCM	chr1	10304208	Intron	novel		0.28
SKCM	chr1	10304490	Intron	novel		0.65
SKCM	chr1	10304240	Intron	novel		0.37
SKCM	chr1	10232369	Missense_Mutation	novel	P14L	0.42
SKCM	chr1	10326318	Silent	novel	D961D	0.52
SKCM	chr1	10256286	Missense_Mutation	NA	S49F	0.19
SKCM	chr1	10282424	Missense_Mutation	NA	S442F	0.17
SKCM	chr1	10343259	Silent	novel	F1220F	0.08
SKCM	chr1	10374333	Missense_Mutation	NA	S1655F	0.21
SKCM	chr1	10371223	Missense_Mutation	NA	P1636L	0.33
SKCM	chr1	10343259	Silent	novel	F1220F	0.49
SKCM	chr1	10292083	Silent	novel	R517R	0.37
SKCM	chr1	10303649	Intron	novel		0.38
SKCM	chr1	10304400	Intron	novel		0.42
SKCM	chr1	10363287	Nonsense_Mutation	novel	R1437*	0.38
SKCM	chr1	10365609	Silent	rs750386624	I1571I	0.41
SKCM	chr1	10275458	Missense_Mutation	NA	P305S	0.74
STAD	chr1	10324830	Silent	rs775697231	S870S	0.29
STAD	chr1	10339801	Missense_Mutation	rs775773486	T1152M	0.33
STAD	chr1	10296978	Missense_Mutation	rs771169398	P648H	0.17
STAD	chr1	10326142	Missense_Mutation	NA	R903C	0.18
STAD	chr1	10258499	Missense_Mutation	NA	D64N	0.14
STAD	chr1	10296636	Missense_Mutation	NA	R611K	0.12
STAD	chr1	10304012	Intron	novel		0.27
STAD	chr1	10303601	Intron	rs144457296		0.31
STAD	chr1	10339792	Missense_Mutation	NA	A1149E	0.3
STAD	chr1	10303570	Intron	rs368503281		0.23
STAD	chr1	10363305	Missense_Mutation	NA	E1443K	0.38
STAD	chr1	10261921	Missense_Mutation	NA	F127C	0.43
STAD	chr1	10295683	Missense_Mutation	rs201531774	R565Q	0.45
STAD	chr1	10304051	Intron	rs377168351		0.14
STAD	chr1	10339802	Silent	rs574168097	T1152T	0.14
STAD	chr1	10347812	Frame_Shift_Ins	novel	*L1285Ffs17**	0.1
STAD	chr1	10276367	Silent	rs777030180	D335D	0.15
STAD	chr1	10258492	Splice_Site	novel	X62_splice	0.35
STAD	chr1	10295682	Missense_Mutation	rs758740011	R565W	0.38
STAD	chr1	10303600	Intron	rs763448385		0.16
STAD	chr1	10276363	Missense_Mutation	NA	A334V	0.28
STAD	chr1	10365111	In_Frame_Del	novel	R1462del	0.17
STAD	chr1	10334554	Missense_Mutation	rs768340319	V987M	0.06
STAD	chr1	10321753	Missense_Mutation	rs368066001	R752W	0.29
STAD	chr1	10347812	Frame_Shift_Ins	novel	*L1285Ffs17**	0.13
STAD	chr1	10303874	Intron	NA		0.07
STAD	chr1	10347776	Silent	novel	V1271V	0.17
STAD	chr1	10326273	Silent	rs138353787	D946D	0.35
STAD	chr1	10303379	Intron	novel		0.24
STAD	chr1	10321809	Silent	rs749823391	A770A	0.22
STAD	chr1	10324822	Missense_Mutation	NA	D868Y	0.22
STAD	chr1	10371165	Missense_Mutation	rs765259892	R1617W	0.62
TGCT	chr1	10334603	Missense_Mutation	rs755104684	R1003Q	0.22
THCA	chr1	10337095	Missense_Mutation	rs765659089	M1051V	0.31
THCA	chr1	10303351	Intron	novel		0.05
THCA	chr1	10365564	Frame_Shift_Ins	novel	*E1562Hfs4**	0.06
UCEC	chr1	10278000	Missense_Mutation	rs773162220	A351V	0.45
UCEC	chr1	10342070	Missense_Mutation	NA	E1178D	0.26
UCEC	chr1	10365565	Missense_Mutation	rs200255510	A1557T	0.39
UCEC	chr1	10376578	Silent	rs188387287	S1814S	0.33
UCEC	chr1	10303168	Intron	rs374126565		0.36
UCEC	chr1	10303874	Intron	NA		0.28
UCEC	chr1	10304348	Intron	NA		0.34
UCEC	chr1	10374879	Missense_Mutation	NA	L1708I	0.1
UCEC	chr1	10376629	3'UTR	novel		0.29
UCEC	chr1	10256276	Missense_Mutation	novel	A46S	0.13
UCEC	chr1	10277996	Missense_Mutation	NA	R350C	0.38
UCEC	chr1	10295151	Missense_Mutation	novel	K552N	0.18
UCEC	chr1	10320088	Nonsense_Mutation	novel	R721*	0.23
UCEC	chr1	10348697	Missense_Mutation	rs762078299	E1305K	0.22
UCEC	chr1	10360989	Silent	novel	N1372N	0.4
UCEC	chr1	10337189	Missense_Mutation	rs745363423	R1082Q	0.34
UCEC	chr1	10365482	Missense_Mutation	rs781051649	S1529L	0.34
UCEC	chr1	10374969	Missense_Mutation	novel	D1738Y	0.08
UCEC	chr1	10320088	Nonsense_Mutation	novel	R721*	0.25
UCEC	chr1	10326295	Missense_Mutation	novel	D954Y	0.33
UCEC	chr1	10368468	Missense_Mutation	novel	C1585Y	0.42
UCEC	chr1	10377138	3'UTR	novel		0.24
UCEC	chr1	10267394	Silent	novel	E148E	0.06
UCEC	chr1	10361825	Missense_Mutation	rs776370957	S1435L	0.44
UCEC	chr1	10375288	Missense_Mutation	rs769837316	R1775C	0.44
UCEC	chr1	10365184	Missense_Mutation	NA	R1484L	0.45
UCEC	chr1	10282517	Missense_Mutation	novel	A473V	0.41
UCEC	chr1	10297013	Missense_Mutation	novel	T660P	0.44
UCEC	chr1	10374345	Missense_Mutation	novel	S1659I	0.08
UCEC	chr1	10295152	Missense_Mutation	novel	D553Y	0.46
UCEC	chr1	10374933	Missense_Mutation	rs754479325	R1726C	0.38
UCEC	chr1	10324822	Missense_Mutation	NA	D868Y	0.14
UCEC	chr1	10304559	Intron	NA		0.27
UCEC	chr1	10304134	Intron	novel		0.03
UCEC	chr1	10296993	Missense_Mutation	novel	P653H	0.28
UCEC	chr1	10348696	Silent	rs775203595	S1304S	0.22
UCEC	chr1	10374452	Nonsense_Mutation	NA	E1695*	0.12
UCEC	chr1	10279111	Missense_Mutation	novel	D399N	0.17
UCEC	chr1	10296921	Missense_Mutation	novel	N629S	0.3
UCEC	chr1	10275466	Silent	novel	R307R	0.05
UCEC	chr1	10297011	Missense_Mutation	NA	W659L	0.32
UCEC	chr1	10345893	Missense_Mutation	NA	S1246N	0.48
UCEC	chr1	10377138	3'UTR	novel		0.72
UCEC	chr1	10292114	Missense_Mutation	novel	P528T	0.16
UCEC	chr1	10380706	3'UTR	novel		0.43
UCEC	chr1	10377276	3'UTR	novel		0.37
UCEC	chr1	10291131	Missense_Mutation	novel	L495P	0.4
UCEC	chr1	10337189	Missense_Mutation	rs745363423	R1082Q	0.14
UCEC	chr1	10377379	3'UTR	novel		0.5
UCEC	chr1	10339774	Missense_Mutation	novel	L1143S	0.16
UCEC	chr1	10361797	Missense_Mutation	novel	G1426C	0.15
UCEC	chr1	10375325	Missense_Mutation	novel	M1787T	0.34
UCEC	chr1	10267414	Missense_Mutation	rs752393884	R155Q	0.34
UCEC	chr1	10295686	Missense_Mutation	rs751881065	R566H	0.33
UCEC	chr1	10321787	Missense_Mutation	rs756162064	R763Q	0.44
UCEC	chr1	10324851	Silent	rs200060590	S877S	0.36
UCEC	chr1	10376598	3'UTR	rs753683228		0.39
UCEC	chr1	10379946	3'UTR	novel		0.45
UCEC	chr1	10381039	3'UTR	novel		1
UCEC	chr1	10320089	Missense_Mutation	rs763303622	R721Q	0.32
UCEC	chr1	10379334	3'UTR	novel		0.24
UCEC	chr1	10380706	3'UTR	novel		0.73
UCEC	chr1	10277997	Missense_Mutation	rs565984994	R350H	0.37
UCEC	chr1	10381458	3'UTR	novel		0.25
UCEC	chr1	10304132	Intron	novel		0.25
UCEC	chr1	10380720	3'UTR	novel		0.29
UCEC	chr1	10275497	Missense_Mutation	novel	N318H	0.42
UCEC	chr1	10282352	Missense_Mutation	novel	R418I	0.43
UCEC	chr1	10304371	Intron	novel		0.43
UCEC	chr1	10304457	Intron	rs773381645		0.4
UCEC	chr1	10348719	Missense_Mutation	rs766432835	R1312H	0.48
UCEC	chr1	10374421	Silent	rs763518005	N1684N	0.4
UCEC	chr1	10378457	3'UTR	novel		0.41
UCEC	chr1	10379180	3'UTR	rs550239533		0.55
UCEC	chr1	10361777	Missense_Mutation	rs567728453	R1419H	0.11
UCEC	chr1	10365482	Missense_Mutation	rs781051649	S1529L	0.22
UCEC	chr1	10304026	Intron	NA		0.29
UCEC	chr1	10256297	Missense_Mutation	novel	D53N	0.49
UCEC	chr1	10267499	Missense_Mutation	novel	K183N	0.43
UCEC	chr1	10297072	Missense_Mutation	NA	E679D	0.42
UCEC	chr1	10303594	Intron	rs200862338		0.4
UCEC	chr1	10303728	Intron	novel		0.56
UCEC	chr1	10320051	Silent	novel	E708E	0.54
UCEC	chr1	10323990	Missense_Mutation	rs766572494	R822H	0.46
UCEC	chr1	10381375	3'UTR	novel		0.44
UCEC	chr1	10361006	Missense_Mutation	NA	G1378V	0.41
UCEC	chr1	10297053	Missense_Mutation	NA	D673G	0.45
UCEC	chr1	10378574	3'UTR	novel		0.11
UCEC	chr1	10258536	Missense_Mutation	NA	D76G	0.38
UCEC	chr1	10376634	3'UTR	novel		0.43
UCEC	chr1	10304334	Intron	novel		0.36
UCEC	chr1	10268164	Silent	novel	A207A	0.25
UCEC	chr1	10292073	Missense_Mutation	novel	V514A	0.43
UCEC	chr1	10303629	Intron	novel		0.17
UCEC	chr1	10377163	3'UTR	novel		0.43
UCEC	chr1	10378490	3'UTR	novel		0.26
UCEC	chr1	10380706	3'UTR	novel		0.58
UCEC	chr1	10256296	Silent	rs764651787	F52F	0.12
UCEC	chr1	10268237	Missense_Mutation	novel	N232D	0.35
UCEC	chr1	10297060	Missense_Mutation	novel	K675N	0.55
UCEC	chr1	10363305	Missense_Mutation	NA	E1443K	0.21
UCEC	chr1	10371159	Missense_Mutation	rs372421679	I1615V	0.19
UCEC	chr1	10371256	Missense_Mutation	novel	D1647G	0.39
UCEC	chr1	10376661	3'UTR	novel		0.27
UCEC	chr1	10377214	3'UTR	novel		0.11
UCEC	chr1	10365565	Missense_Mutation	rs200255510	A1557T	0.36
UCEC	chr1	10374922	Missense_Mutation	novel	F1722S	0.4
UCEC	chr1	10379988	3'UTR	novel		0.38
UCEC	chr1	10380280	3'UTR	rs556013366		0.35
UCEC	chr1	10381200	3'UTR	novel		0.5
UCEC	chr1	10303937	Intron	novel		0.57
UCEC	chr1	10380706	3'UTR	novel		0.47
UCEC	chr1	10323989	Missense_Mutation	rs760896802	R822C	0.35
UCEC	chr1	10365161	Missense_Mutation	novel	E1476D	0.44
UCEC	chr1	10275449	Missense_Mutation	novel	D302Y	0.35
UCEC	chr1	10296608	Missense_Mutation	rs767848662	R602C	0.29
UCEC	chr1	10268190	Missense_Mutation	novel	R216H	0.19
UCEC	chr1	10374336	Missense_Mutation	rs373439616	R1656Q	0.36
UCEC	chr1	10272260	Missense_Mutation	novel	K273T	0.33
UCEC	chr1	10304457	Intron	rs773381645		0.4
UCEC	chr1	10375284	Silent	novel	K1773K	0.53
UCEC	chr1	10304490	Intron	novel		0.56
UCEC	chr1	10326310	Missense_Mutation	rs764910038	G959R	0.36
UCEC	chr1	10277996	Missense_Mutation	NA	R350C	0.14
UCEC	chr1	10296586	Silent	rs774839409	I594I	0.14
UCEC	chr1	10304426	Intron	novel		0.12
UCEC	chr1	10334581	Missense_Mutation	rs145596547	V996I	0.29
UCEC	chr1	10381367	3'UTR	novel		0.08
UCEC	chr1	10303599	Intron	novel		0.18
UCEC	chr1	10375372	Missense_Mutation	rs759957126	R1803W	0.39
UCEC	chr1	10378360	3'UTR	novel		0.1
UCEC	chr1	10380706	3'UTR	novel		0.35
UCEC	chr1	10258586	Frame_Shift_Ins	novel	*A95Cfs16**	0.24
UCEC	chr1	10375289	Missense_Mutation	rs374303355	R1775H	0.26
UCEC	chr1	10256263	Missense_Mutation	NA	K41N	0.51
UCEC	chr1	10348659	Missense_Mutation	NA	R1292Q	0.05
UCEC	chr1	10360961	Missense_Mutation	novel	S1363N	0.05
UCEC	chr1	10303967	Intron	NA		0.23
UCEC	chr1	10320125	Missense_Mutation	NA	E733A	0.28
UCEC	chr1	10275436	Missense_Mutation	NA	K297N	0.27
UCEC	chr1	10303241	Intron	novel		0.36
UCEC	chr1	10377298	3'UTR	novel		0.28
UCEC	chr1	10297189	Silent	novel	E686E	0.09
UCEC	chr1	10267392	Nonsense_Mutation	novel	E148*	0.2
UCEC	chr1	10303306	Intron	novel		0.24
UCEC	chr1	10336707	Missense_Mutation	novel	A1032S	0.19
UCEC	chr1	10337415	Missense_Mutation	novel	G1102W	0.24
UCEC	chr1	10365107	Missense_Mutation	novel	Q1458H	0.19
UCEC	chr1	10374981	Missense_Mutation	rs200161482	R1742C	0.3
UCEC	chr1	10376651	3'UTR	novel		0.54
UCEC	chr1	10303967	Intron	NA		0.32
UCEC	chr1	10326321	Silent	rs763515223	P962P	0.41
UCEC	chr1	10363292	Silent	novel	V1438V	0.52
UCEC	chr1	10268208	Missense_Mutation	novel	T222M	0.14
UCEC	chr1	10303437	Intron	novel		0.06
UCEC	chr1	10324852	Missense_Mutation	NA	D878N	0.3
UCEC	chr1	10345917	Missense_Mutation	NA	V1254A	0.38
UCEC	chr1	10303186	Intron	rs116859745		0.38
UCEC	chr1	10256296	Silent	rs764651787	F52F	0.42
UCEC	chr1	10303883	Intron	novel		0.41
UCEC	chr1	10375354	Missense_Mutation	novel	L1797F	0.33
UCEC	chr1	10381458	3'UTR	novel		0.48
UCEC	chr1	10347797	Silent	novel	L1278L	0.4
UCEC	chr1	10375025	Missense_Mutation	novel	E1756D	0.35
UCEC	chr1	10376661	3'UTR	novel		0.25
UCEC	chr1	10379284	3'UTR	rs756359695		0.55
UCEC	chr1	10380755	3'UTR	novel		0.28
UCS	chr1	10304474	Intron	rs146807975		0.41
UCS	chr1	10258538	Missense_Mutation	novel	I77L	0.06

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
CESC	DEL	0.1051	0.00029523
CHOL	DEL	0.8056	3.3987e-23
DLBC	DEL	0.1042	0.011841
HNSC	DEL	0.1398	7.0766e-07
KIRC	DEL	0.1439	2.3538e-09
KIRP	DEL	0.1736	1.462e-09
LUAD	DEL	0.1415	0.0024765
LUSC	DEL	0.3573	2.5882e-07
MESO	DEL	0.3448	2.434e-07
READ	DEL	0.3939	2.1758e-10
TGCT	DEL	0.18	0.00046313
UCS	DEL	0.3036	0.0051125

Survival Analysis

Cancer	P-value	Q-value
THYM	0.024	Kaplan-Meier Survival Analysis
SARC	0.0021	Kaplan-Meier Survival Analysis
ACC	0.0013	Kaplan-Meier Survival Analysis
KIRP	0.011	Kaplan-Meier Survival Analysis
COAD	0.04	Kaplan-Meier Survival Analysis
PAAD	0.026	Kaplan-Meier Survival Analysis
BLCA	0.0023	Kaplan-Meier Survival Analysis
CESC	0.044	Kaplan-Meier Survival Analysis
KICH	0.027	Kaplan-Meier Survival Analysis
UCEC	0.018	Kaplan-Meier Survival Analysis
LIHC	0.042	Kaplan-Meier Survival Analysis
LGG	0.023	Kaplan-Meier Survival Analysis
LUAD	0.016	Kaplan-Meier Survival Analysis
UVM	0.032	Kaplan-Meier Survival Analysis
OV	0.011	Kaplan-Meier Survival Analysis

Drugs

EuRBPDB

Description

RBPome

Literatures

Expression

Transcripts

Gene Model

Phenotypes

GWAS

PPI

Orthologs

Gene Ontology

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Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742