Primary Site >> Stomach Cancer

Gene >> CD19

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324662
Start 28935539:28935539(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.931C>A
AA Mutation p.Leu311Ile(p.L311I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324662
Start 28936174:28936174(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.968G>T
AA Mutation p.Arg323Ile(p.R323I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324662
Start 28932358:28932358(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.101C>T
AA Mutation p.Ala34Val(p.A34V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000324662
Start 28937350:28937350(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1278C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000324662
Start 28937326:28937326(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768949308
CDS Mutation c.1254C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000324662
Start 28932554:28932554(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368196796
CDS Mutation c.297G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000324662
Start 28932605:28932605(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.348G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000324662
Start 28932558:28932558(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.306delC
AA Mutation p.Ser103LeufsTer27(p.S103Lfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000324662
Start 28932530:28932530(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.278delG
AA Mutation p.Gly93AlafsTer37(p.G93Afs*37)
Mutation Classification Frame_Shift_Del
Feature Type Transcript