Primary Site >> Stomach Cancer

Gene >> ASL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000304874
Start 66092623:66092623(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757216794
CDS Mutation c.1210G>A
AA Mutation p.Ala404Thr(p.A404T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000304874
Start 66092815:66092815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1298G>T
AA Mutation p.Ser433Ile(p.S433I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000304874
Start 66089161:66089161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.904C>T
AA Mutation p.Arg302Cys(p.R302C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000304874
Start 66081866:66081866(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775839623
CDS Mutation c.76G>A
AA Mutation p.Ala26Thr(p.A26T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000304874
Start 66082896:66082896(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768087423
CDS Mutation c.308C>T
AA Mutation p.Thr103Met(p.T103M)
Mutation Classification Missense_Mutation
Feature Type Transcript