Primary Site >> Stomach Cancer
Gene >> BRD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32977896:32977896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469C>G |
| AA Mutation | p.Ser490Cys(p.S490C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32980067:32980067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2081C>A |
| AA Mutation | p.Ser694Tyr(p.S694Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32980411:32980411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2216G>A |
| AA Mutation | p.Arg739Gln(p.R739Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32976914:32976914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1178C>A |
| AA Mutation | p.Pro393His(p.P393H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32979845:32979845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1859C>G |
| AA Mutation | p.Thr620Arg(p.T620R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32978247:32978247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1700C>T |
| AA Mutation | p.Ala567Val(p.A567V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32979929:32979929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1943G>A |
| AA Mutation | p.Arg648Gln(p.R648Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32977854:32977854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756721721 |
| CDS Mutation | c.1427C>T |
| AA Mutation | p.Ser476Leu(p.S476L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32980086:32980086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2100G>T |
| AA Mutation | p.Glu700Asp(p.E700D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32976364:32976364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.725A>G |
| AA Mutation | p.His242Arg(p.H242R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374825 |
| Start | 32976719:32976719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.983G>A |
| AA Mutation | p.Arg328His(p.R328H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374825 |
| Start | 32974490:32974490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.58C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374825 |
| Start | 32976305:32976305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.666A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374825 |
| Start | 32975500:32975500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.450C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374825 |
| Start | 32977900:32977900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1473T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374825 |
| Start | 32977540:32977540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139231674 |
| CDS Mutation | c.1299C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374825 |
| Start | 32976688:32976691(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.956_959delAGAG |
| AA Mutation | p.Glu319ValfsTer31(p.E319Vfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000374825 |
| Start | 32974712:32974712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.280C>T |
| AA Mutation | p.Gln94Ter(p.Q94*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374825 |
| Start | 32976687:32976688(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.958_959dupAG |
| AA Mutation | p.Ser320ArgfsTer32(p.S320Rfs*32) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |