Primary Site >> Stomach Cancer

Gene >> VCP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35059797:35059797(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201431036
CDS Mutation c.1700G>A
AA Mutation p.Arg567His(p.R567H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35065364:35065364(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121909330
CDS Mutation c.463C>T
AA Mutation p.Arg155Cys(p.R155C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35061059:35061059(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1315G>A
AA Mutation p.Ala439Thr(p.A439T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35062116:35062116(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.968G>A
AA Mutation p.Arg323His(p.R323H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35059528:35059528(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1969C>A
AA Mutation p.Leu657Ile(p.L657I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000358901
Start 35066772:35066772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.348G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000358901
Start 35062115:35062115(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.969C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000358901
Start 35059580:35059580(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1917T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000358901
Start 35068347:35068348(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.32_33delAC
AA Mutation p.Asp11AlafsTer18(p.D11Afs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript