Primary Site >> Stomach Cancer

Gene >> ATE1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000224652
Start 121841098:121841098(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs538914300
CDS Mutation c.1141G>A
AA Mutation p.Val381Ile(p.V381I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000224652
Start 121743711:121743711(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1526G>A
AA Mutation p.Cys509Tyr(p.C509Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000224652
Start 121899967:121899967(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745816449
CDS Mutation c.841A>G
AA Mutation p.Ser281Gly(p.S281G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000224652
Start 121841151:121841151(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1088T>A
AA Mutation p.Val363Glu(p.V363E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000224652
Start 121924279:121924279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.157C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000224652
Start 121913838:121913838(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.289delA
AA Mutation p.Met97CysfsTer2(p.M97Cfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript