Primary Site >> Stomach Cancer

Gene >> BCAT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261192
Start 24849933:24849933(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.527A>C
AA Mutation p.Lys176Thr(p.K176T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261192
Start 24901827:24901827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.65T>C
AA Mutation p.Val22Ala(p.V22A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261192
Start 24836522:24836522(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761486552
CDS Mutation c.892G>A
AA Mutation p.Ala298Thr(p.A298T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261192
Start 24894393:24894393(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774269366
CDS Mutation c.161C>T
AA Mutation p.Thr54Met(p.T54M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261192
Start 24842206:24842206(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.693T>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000261192
Start 24894368:24894368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.186G>A
AA Mutation p.Trp62Ter(p.W62*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant
Transcription ID ENST00000261192
Start 24849784:24849784(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.674+2T>C
Mutation Classification Splice_Site
Feature Type Transcript