Primary Site >> Stomach Cancer

Gene >> ACD

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000393919
Start 67657986:67657986(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1464G>T
AA Mutation p.Trp488Cys(p.W488C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000393919
Start 67658042:67658042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746002676
CDS Mutation c.1408C>T
AA Mutation p.Pro470Ser(p.P470S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000393919
Start 67659028:67659028(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.803A>G
AA Mutation p.Gln268Arg(p.Q268R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000393919
Start 67658345:67658345(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1105G>A
AA Mutation p.Gly369Ser(p.G369S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000393919
Start 67660222:67660222(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.257G>T
AA Mutation p.Gly86Val(p.G86V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000393919
Start 67660258:67660258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.221A>G
AA Mutation p.Asn74Ser(p.N74S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000393919
Start 67658759:67658759(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.961C>T
Mutation Classification Silent
Feature Type Transcript