Primary Site >> Stomach Cancer
Gene >> BRAF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140776956:140776956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1650G>A |
| AA Mutation | p.Met550Ile(p.M550I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140800428:140800428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547693139 |
| CDS Mutation | c.914C>T |
| AA Mutation | p.Ala305Val(p.A305V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140753355:140753355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397516896 |
| CDS Mutation | c.1780G>A |
| AA Mutation | p.Asp594Asn(p.D594N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140777057:140777057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1549A>G |
| AA Mutation | p.Met517Val(p.M517V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140781602:140781602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913355 |
| CDS Mutation | c.1406G>C |
| AA Mutation | p.Gly469Ala(p.G469A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140776919:140776919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1687G>T |
| AA Mutation | p.Gly563Cys(p.G563C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140754226:140754226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1702C>G |
| AA Mutation | p.His568Asp(p.H568D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140734613:140734613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775889922 |
| CDS Mutation | c.2285C>T |
| AA Mutation | p.Ala762Val(p.A762V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140753333:140753333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397507484 |
| CDS Mutation | c.1802A>C |
| AA Mutation | p.Lys601Thr(p.K601T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288602 |
| Start | 140734764:140734764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2134G>A |
| AA Mutation | p.Ala712Thr(p.A712T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288602 |
| Start | 140834654:140834654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.459A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288602 |
| Start | 140801456:140801456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.816T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288602 |
| Start | 140794368:140794368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1080A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288602 |
| Start | 140834720:140834720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.393A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288602 |
| Start | 140754215:140754215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1713A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288602 |
| Start | 140778041:140778041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1467A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000288602 |
| Start | 140783127:140783127(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1208delC |
| AA Mutation | p.Pro403LeufsTer8(p.P403Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000288602 |
| Start | 140753328:140753328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs104886015 |
| CDS Mutation | c.1807C>T |
| AA Mutation | p.Arg603Ter(p.R603*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |