Primary Site >> Stomach Cancer

Gene >> BPI

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262865
Start 38304305:38304305(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776005510
CDS Mutation c.94G>A
AA Mutation p.Val32Ile(p.V32I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262865
Start 38310598:38310598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.494G>A
AA Mutation p.Ser165Asn(p.S165N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262865
Start 38304290:38304290(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs549000920
CDS Mutation c.79G>A
AA Mutation p.Ala27Thr(p.A27T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262865
Start 38326367:38326367(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144369430
CDS Mutation c.1108G>A
AA Mutation p.Val370Met(p.V370M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262865
Start 38307629:38307629(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.205T>A
AA Mutation p.Ser69Thr(p.S69T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000262865
Start 38334462:38334462(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1317T>C
Mutation Classification Silent
Feature Type Transcript