Primary Site >> Stomach Cancer

Gene >> VPREB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000403807
Start 22245110:22245110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.211T>A
AA Mutation p.Tyr71Asn(p.Y71N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000403807
Start 22245195:22245195(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143361893
CDS Mutation c.296A>G
AA Mutation p.Tyr99Cys(p.Y99C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000403807
Start 22244989:22244989(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.90C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000403807
Start 22244825:22244825(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12T>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000403807
Start 22244962:22244962(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs555986282
CDS Mutation c.63G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000403807
Start 22244974:22244974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.75G>A
Mutation Classification Silent
Feature Type Transcript