Primary Site >> Stomach Cancer

Gene >> BRD7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394688
Start 50323660:50323660(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1370A>T
AA Mutation p.Tyr457Phe(p.Y457F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394688
Start 50328710:50328710(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1046C>T
AA Mutation p.Thr349Met(p.T349M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394688
Start 50354468:50354468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.403C>T
AA Mutation p.Pro135Ser(p.P135S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000394688
Start 50368257:50368257(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.91G>T
AA Mutation p.Gly31Trp(p.G31W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000394688
Start 50320749:50320749(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143187051
CDS Mutation c.1526G>A
AA Mutation p.Arg509His(p.R509H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000394688
Start 50354895:50354895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.286C>T
AA Mutation p.Arg96Trp(p.R96W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000394688
Start 50323689:50323689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1341G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000394688
Start 50320294:50320294(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148031885
CDS Mutation c.1710G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000394688
Start 50320712:50320712(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1563G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000394688
Start 50354907:50354907(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.274C>T
AA Mutation p.Arg92Ter(p.R92*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000394688
Start 50350168:50350168(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.447-1G>T
Mutation Classification Splice_Site
Feature Type Transcript