Primary Site >> Stomach Cancer

Gene >> CD247

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000362089
Start 167439382:167439382(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.181G>A
AA Mutation p.Ala61Thr(p.A61T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000362089
Start 167439357:167439357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.206A>G
AA Mutation p.Asn69Ser(p.N69S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000362089
Start 167439378:167439378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.185C>A
AA Mutation p.Pro62His(p.P62H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000362089
Start 167431713:167431713(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs561262982
CDS Mutation c.463G>A
AA Mutation p.Ala155Thr(p.A155T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000362089
Start 167431696:167431696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.480C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000362089
Start 167435426:167435426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.309G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000362089
Start 167433049:167433049(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.404delG
AA Mutation p.Gly135AlafsTer65(p.G135Afs*65)
Mutation Classification Frame_Shift_Del
Feature Type Transcript