Primary Site >> Stomach Cancer

Gene >> BNIP3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368636
Start 131970726:131970726(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.451A>G
AA Mutation p.Met151Val(p.M151V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368636
Start 131970688:131970688(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.489A>C
AA Mutation p.Lys163Asn(p.K163N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368636
Start 131970762:131970762(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376910597
CDS Mutation c.415C>T
AA Mutation p.Arg139Cys(p.R139C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368636
Start 131973800:131973800(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.190T>G
AA Mutation p.Cys64Gly(p.C64G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000368636
Start 131973885:131973885(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755528330
CDS Mutation c.105G>A
Mutation Classification Silent
Feature Type Transcript