Primary Site >> Stomach Cancer

Gene >> BCL2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000333681
Start 63318528:63318528(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368344129
CDS Mutation c.139G>A
AA Mutation p.Gly47Ser(p.G47S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000333681
Start 63318486:63318486(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772554403
CDS Mutation c.181G>A
AA Mutation p.Ala61Thr(p.A61T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000333681
Start 63318325:63318325(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.342G>T
AA Mutation p.Glu114Asp(p.E114D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000333681
Start 63318284:63318284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.383G>A
AA Mutation p.Gly128Glu(p.G128E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000333681
Start 63318374:63318374(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.293G>A
AA Mutation p.Arg98His(p.R98H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000333681
Start 63318556:63318556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.111C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000333681
Start 63318166:63318166(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.501G>A
Mutation Classification Silent
Feature Type Transcript