Primary Site >> Stomach Cancer

Gene >> A1BG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263100
Start 58351543:58351543(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.758C>A
AA Mutation p.Pro253His(p.P253H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263100
Start 58351484:58351484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.817G>A
AA Mutation p.Asp273Asn(p.D273N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263100
Start 58347392:58347392(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1441G>A
AA Mutation p.Glu481Lys(p.E481K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263100
Start 58352514:58352514(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.382T>C
AA Mutation p.Trp128Arg(p.W128R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263100
Start 58351510:58351510(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.791T>C
AA Mutation p.Phe264Ser(p.F264S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000263100
Start 58352461:58352461(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.435T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000263100
Start 58351410:58351410(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.891C>T
Mutation Classification Silent
Feature Type Transcript