Primary Site >> Stomach Cancer
Gene >> SEMA5A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9197272:9197272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.964T>C |
| AA Mutation | p.Phe322Leu(p.F322L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9108184:9108184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147869499 |
| CDS Mutation | c.2029C>T |
| AA Mutation | p.Arg677Cys(p.R677C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9063026:9063026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2379G>C |
| AA Mutation | p.Trp793Cys(p.W793C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9136511:9136511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202102793 |
| CDS Mutation | c.1592C>T |
| AA Mutation | p.Ala531Val(p.A531V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9224752:9224752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753154714 |
| CDS Mutation | c.568C>T |
| AA Mutation | p.Arg190Cys(p.R190C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9066469:9066469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2251G>A |
| AA Mutation | p.Glu751Lys(p.E751K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9063030:9063030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2290734 |
| CDS Mutation | c.2375C>T |
| AA Mutation | p.Ser792Leu(p.S792L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9154637:9154637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1332G>T |
| AA Mutation | p.Leu444Phe(p.L444F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9154690:9154690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751530635 |
| CDS Mutation | c.1279G>A |
| AA Mutation | p.Gly427Arg(p.G427R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9044416:9044416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3062A>C |
| AA Mutation | p.His1021Pro(p.H1021P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9226925:9226925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370111417 |
| CDS Mutation | c.376G>A |
| AA Mutation | p.Asp126Asn(p.D126N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9066603:9066603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2117A>C |
| AA Mutation | p.Lys706Thr(p.K706T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9226888:9226888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.413C>G |
| AA Mutation | p.Pro138Arg(p.P138R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9202211:9202211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140433904 |
| CDS Mutation | c.676G>A |
| AA Mutation | p.Gly226Arg(p.G226R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9063060:9063060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763496362 |
| CDS Mutation | c.2345C>T |
| AA Mutation | p.Thr782Met(p.T782M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9226934:9226934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.367G>T |
| AA Mutation | p.Val123Leu(p.V123L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9063067:9063067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2338G>A |
| AA Mutation | p.Ala780Thr(p.A780T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9063045:9063045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2360G>C |
| AA Mutation | p.Trp787Ser(p.W787S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9136554:9136554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1549G>C |
| AA Mutation | p.Glu517Gln(p.E517Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9197254:9197254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773789880 |
| CDS Mutation | c.982G>A |
| AA Mutation | p.Ala328Thr(p.A328T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9044461:9044461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3017T>C |
| AA Mutation | p.Ile1006Thr(p.I1006T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9136585:9136585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1518G>T |
| AA Mutation | p.Trp506Cys(p.W506C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9190393:9190393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1147C>T |
| AA Mutation | p.His383Tyr(p.H383Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382496 |
| Start | 9122777:9122777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1660C>T |
| AA Mutation | p.His554Tyr(p.H554Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9154508:9154508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1461C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9042918:9042918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3204C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9054196:9054196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2580A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9054130:9054130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2646G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9052018:9052018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755737357 |
| CDS Mutation | c.2700G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9054250:9054250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2526C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9066515:9066515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2205C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9044394:9044394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561198451 |
| CDS Mutation | c.3084C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9108215:9108215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1998A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9044505:9044505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2973T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382496 |
| Start | 9197276:9197276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377749349 |
| CDS Mutation | c.960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |