Primary Site >> Stomach Cancer

Gene >> GPT

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394955
Start 144506017:144506017(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.842C>T
AA Mutation p.Ala281Val(p.A281V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394955
Start 144504652:144504652(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751740696
CDS Mutation c.211G>A
AA Mutation p.Ala71Thr(p.A71T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394955
Start 144504780:144504780(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.262C>A
AA Mutation p.Leu88Ile(p.L88I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000394955
Start 144505056:144505056(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375120964
CDS Mutation c.420T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000394955
Start 144504460:144504460(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.156G>A
Mutation Classification Silent
Feature Type Transcript