Mutation

Primary Site >> Stomach Cancer

Gene >> DOCK11

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118590298:118590298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2135A>G
AA Mutation	p.Asp712Gly(p.D712G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118662710:118662710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146074785
CDS Mutation	c.4994C>T
AA Mutation	p.Ala1665Val(p.A1665V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000276202
Start	118614692:118614692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377535991
CDS Mutation	c.3097C>T
AA Mutation	p.Arg1033Cys(p.R1033C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118610303:118610303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2981A>T
AA Mutation	p.Tyr994Phe(p.Y994F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118671134:118671134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764343924
CDS Mutation	c.5188C>T
AA Mutation	p.Arg1730Cys(p.R1730C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118662724:118662724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5008A>T
AA Mutation	p.Thr1670Ser(p.T1670S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118654687:118654687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4781A>T
AA Mutation	p.Glu1594Val(p.E1594V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118654622:118654622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4716A>C
AA Mutation	p.Glu1572Asp(p.E1572D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118543545:118543545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344T>C
AA Mutation	p.Val115Ala(p.V115A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000276202
Start	118683182:118683182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113662446
CDS Mutation	c.6067A>G
AA Mutation	p.Met2023Val(p.M2023V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000276202
Start	118639437:118639437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4004T>C
AA Mutation	p.Val1335Ala(p.V1335A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276202
Start	118588303:118588303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1962C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276202
Start	118685795:118685795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766552795
CDS Mutation	c.6210C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276202
Start	118561496:118561496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112113377
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276202
Start	118630408:118630408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3804A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276202
Start	118636377:118636377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3918A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276202
Start	118588463:118588463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755060885
CDS Mutation	c.2031C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276202
Start	118610275:118610275(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2956delC
AA Mutation	p.Arg986GlufsTer20(p.R986Efs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276202
Start	118598084:118598084(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2443delA
AA Mutation	p.Ser815AlafsTer3(p.S815Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000276202
Start	118662745:118662745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5029G>T
AA Mutation	p.Gly1677Ter(p.G1677*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000276202
Start	118618729:118618729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3471+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000276202
Start	118608070:118608070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2682-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000276202
Start	118593339:118593339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2263+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	24
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000276202
Start	118566573:118566573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript