Primary Site >> Stomach Cancer

Gene >> CAPG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263867
Start 85395623:85395623(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761175093
CDS Mutation c.896G>A
AA Mutation p.Arg299Gln(p.R299Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263867
Start 85401224:85401224(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs185763147
CDS Mutation c.457C>T
AA Mutation p.Arg153Trp(p.R153W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263867
Start 85401287:85401287(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.394G>A
AA Mutation p.Ala132Thr(p.A132T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263867
Start 85401923:85401923(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.58G>A
AA Mutation p.Gly20Ser(p.G20S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000263867
Start 85401318:85401318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.363G>A
Mutation Classification Silent
Feature Type Transcript