Primary Site >> Stomach Cancer
Gene >> BRD4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15242930:15242930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3139C>T |
| AA Mutation | p.Arg1047Trp(p.R1047W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15255465:15255465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752762666 |
| CDS Mutation | c.1879G>A |
| AA Mutation | p.Gly627Ser(p.G627S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15244371:15244371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2441G>A |
| AA Mutation | p.Gly814Asp(p.G814D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15238919:15238919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750347317 |
| CDS Mutation | c.3844C>T |
| AA Mutation | p.Arg1282Cys(p.R1282C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15255551:15255551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138134048 |
| CDS Mutation | c.1793C>T |
| AA Mutation | p.Thr598Met(p.T598M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15255359:15255359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1985C>T |
| AA Mutation | p.Ser662Phe(p.S662F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15265638:15265638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.565G>A |
| AA Mutation | p.Ala189Thr(p.A189T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15243004:15243004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780028668 |
| CDS Mutation | c.3065C>T |
| AA Mutation | p.Pro1022Leu(p.P1022L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15256218:15256218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1597C>A |
| AA Mutation | p.Gln533Lys(p.Q533K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15239132:15239132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3709C>T |
| AA Mutation | p.Arg1237Cys(p.R1237C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15239402:15239402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368540009 |
| CDS Mutation | c.3566C>T |
| AA Mutation | p.Ala1189Val(p.A1189V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15243359:15243359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2710C>T |
| AA Mutation | p.Pro904Ser(p.P904S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15243244:15243244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765227557 |
| CDS Mutation | c.2825C>T |
| AA Mutation | p.Thr942Met(p.T942M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15244320:15244320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2492C>T |
| AA Mutation | p.Pro831Leu(p.P831L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15254213:15254213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200566617 |
| CDS Mutation | c.2097G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15265618:15265618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183675300 |
| CDS Mutation | c.585G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15265627:15265627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763875252 |
| CDS Mutation | c.576C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15268998:15268998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.330A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15272962:15272962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139655217 |
| CDS Mutation | c.138G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15257069:15257069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750121394 |
| CDS Mutation | c.1446G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |