Primary Site >> Stomach Cancer

Gene >> AIM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368130
Start 159066269:159066269(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.457T>C
AA Mutation p.Cys153Arg(p.C153R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368130
Start 159073415:159073415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85C>A
AA Mutation p.Leu29Ile(p.L29I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368130
Start 159066238:159066238(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.488A>C
AA Mutation p.Lys163Thr(p.K163T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000368130
Start 159073326:159073326(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760542046
CDS Mutation c.174G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000368130
Start 159065928:159065928(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.798T>G
Mutation Classification Silent
Feature Type Transcript