Primary Site >> Stomach Cancer

Gene >> GLIS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262366
Start 4336991:4336991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1042G>A
AA Mutation p.Val348Ile(p.V348I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262366
Start 4334877:4334877(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.422C>G
AA Mutation p.Ala141Gly(p.A141G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262366
Start 4335325:4335325(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372555307
CDS Mutation c.707G>A
AA Mutation p.Arg236His(p.R236H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262366
Start 4332337:4332337(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199506809
CDS Mutation c.57G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262366
Start 4334893:4334893(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.438C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000262366
Start 4334870:4334870(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.421delG
AA Mutation p.Ala141ProfsTer110(p.A141Pfs*110)
Mutation Classification Frame_Shift_Del
Feature Type Transcript