Primary Site >> Stomach Cancer
Gene >> SEMA4D
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89388784:89388784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.959T>C |
| AA Mutation | p.Val320Ala(p.V320A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89396793:89396793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745686318 |
| CDS Mutation | c.358G>A |
| AA Mutation | p.Ala120Thr(p.A120T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89379308:89379308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1985A>G |
| AA Mutation | p.Gln662Arg(p.Q662R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89393606:89393606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.464G>A |
| AA Mutation | p.Arg155Lys(p.R155K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89402890:89402890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.233T>C |
| AA Mutation | p.Ile78Thr(p.I78T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89393571:89393571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759275072 |
| CDS Mutation | c.499G>A |
| AA Mutation | p.Val167Ile(p.V167I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89387446:89387446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542114524 |
| CDS Mutation | c.1270G>A |
| AA Mutation | p.Val424Met(p.V424M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89396750:89396750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.401C>A |
| AA Mutation | p.Ala134Asp(p.A134D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89388674:89388674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1069C>T |
| AA Mutation | p.Arg357Cys(p.R357C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89379336:89379336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753165801 |
| CDS Mutation | c.1957G>A |
| AA Mutation | p.Val653Ile(p.V653I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89405371:89405371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.86G>A |
| AA Mutation | p.Arg29Gln(p.R29Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356444 |
| Start | 89378853:89378853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756135411 |
| CDS Mutation | c.2440G>A |
| AA Mutation | p.Gly814Ser(p.G814S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356444 |
| Start | 89388726:89388726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1017C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356444 |
| Start | 89391318:89391318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.720G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356444 |
| Start | 89379577:89379577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1716G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356444 |
| Start | 89405394:89405394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780457676 |
| CDS Mutation | c.63G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356444 |
| Start | 89388943:89388943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.879G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356444 |
| Start | 89381221:89381221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142877769 |
| CDS Mutation | c.1572G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356444 |
| Start | 89386445:89386445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779094970 |
| CDS Mutation | c.1368C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |