Mutation

Primary Site >> Stomach Cancer

Gene >> WDR62

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36103586:36103586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778175384
CDS Mutation	c.3743C>T
AA Mutation	p.Ser1248Leu(p.S1248L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36104993:36104993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4522G>T
AA Mutation	p.Val1508Leu(p.V1508L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36103382:36103382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3539C>T
AA Mutation	p.Ser1180Phe(p.S1180F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36066005:36066005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380T>C
AA Mutation	p.Val127Ala(p.V127A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36067315:36067315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768099287
CDS Mutation	c.571G>A
AA Mutation	p.Val191Ile(p.V191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36067436:36067436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692A>G
AA Mutation	p.Glu231Gly(p.E231G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36104928:36104928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542711912
CDS Mutation	c.4457C>T
AA Mutation	p.Pro1486Leu(p.P1486L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36089092:36089092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774588484
CDS Mutation	c.1823G>A
AA Mutation	p.Arg608His(p.R608H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36099465:36099465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764299399
CDS Mutation	c.2587C>T
AA Mutation	p.Arg863Cys(p.R863C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36103058:36103058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3431C>T
AA Mutation	p.Ser1144Phe(p.S1144F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36092780:36092780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532692601
CDS Mutation	c.2302A>G
AA Mutation	p.Thr768Ala(p.T768A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36067955:36067955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827G>C
AA Mutation	p.Gly276Ala(p.G276A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36091240:36091240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2075G>A
AA Mutation	p.Cys692Tyr(p.C692Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36103552:36103552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143493857
CDS Mutation	c.3709G>A
AA Mutation	p.Val1237Met(p.V1237M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36103709:36103709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773029330
CDS Mutation	c.3866G>A
AA Mutation	p.Arg1289Gln(p.R1289Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36073421:36073421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123T>A
AA Mutation	p.Ser375Thr(p.S375T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36103973:36103973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4130C>T
AA Mutation	p.Pro1377Leu(p.P1377L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36104844:36104844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4373A>G
AA Mutation	p.His1458Arg(p.H1458R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36103173:36103173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3465G>T
AA Mutation	p.Lys1155Asn(p.K1155N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36104670:36104670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756795208
CDS Mutation	c.4291C>T
AA Mutation	p.Arg1431Cys(p.R1431C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36092795:36092795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2317C>T
AA Mutation	p.Arg773Trp(p.R773W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000270301
Start	36103862:36103862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774129490
CDS Mutation	c.4019G>A
AA Mutation	p.Arg1340His(p.R1340H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270301
Start	36073516:36073516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766269117
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270301
Start	36102018:36102018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141344823
CDS Mutation	c.3087C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270301
Start	36066358:36066358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270301
Start	36092692:36092692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757339378
CDS Mutation	c.2214C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000270301
Start	36103825:36103825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3982G>T
AA Mutation	p.Glu1328Ter(p.E1328*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000270301
Start	36103076:36103076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3447+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	29
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000270301
Start	36084746:36084746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript