Primary Site >> Stomach Cancer
Gene >> NGF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286558:115286558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778266438 |
| CDS Mutation | c.238C>T |
| AA Mutation | p.Arg80Trp(p.R80W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286637:115286637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.159C>A |
| AA Mutation | p.Ser53Arg(p.S53R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286623:115286623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201861727 |
| CDS Mutation | c.173C>T |
| AA Mutation | p.Ala58Val(p.A58V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286351:115286351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149823633 |
| CDS Mutation | c.445G>A |
| AA Mutation | p.Ala149Thr(p.A149T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286662:115286662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134A>C |
| AA Mutation | p.Asp45Ala(p.D45A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286719:115286719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.77T>C |
| AA Mutation | p.Val26Ala(p.V26A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286299:115286299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497A>C |
| AA Mutation | p.Asn166Thr(p.N166T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286690:115286690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106C>A |
| AA Mutation | p.His36Asn(p.H36N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286354:115286354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.442A>G |
| AA Mutation | p.Thr148Ala(p.T148A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286135:115286135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11466112 |
| CDS Mutation | c.661C>T |
| AA Mutation | p.Arg221Trp(p.R221W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369512 |
| Start | 115286610:115286610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780432648 |
| CDS Mutation | c.186C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |