Primary Site >> Stomach Cancer

Gene >> BHLHE40

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000256495
Start 4983649:4983649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1196C>T
AA Mutation p.Ala399Val(p.A399V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000256495
Start 4983130:4983130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.677C>T
AA Mutation p.Thr226Ile(p.T226I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000256495
Start 4983448:4983448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.995C>T
AA Mutation p.Ala332Val(p.A332V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000256495
Start 4983478:4983478(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1025G>A
AA Mutation p.Cys342Tyr(p.C342Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000256495
Start 4983299:4983299(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767694119
CDS Mutation c.846C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000256495
Start 4981475:4981475(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.342G>A
Mutation Classification Silent
Feature Type Transcript