Primary Site >> Stomach Cancer

Gene >> ZBTB32

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262630
Start 35716144:35716144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1036A>G
AA Mutation p.Thr346Ala(p.T346A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262630
Start 35714699:35714699(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs529757518
CDS Mutation c.73C>T
AA Mutation p.Arg25Trp(p.R25W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262630
Start 35716552:35716552(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1264A>G
AA Mutation p.Thr422Ala(p.T422A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262630
Start 35715443:35715443(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.817G>A
AA Mutation p.Gly273Ser(p.G273S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262630
Start 35716680:35716680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1392C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000262630
Start 35714636:35714636(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.15delC
AA Mutation p.Ile6Ter(p.I6*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript