Primary Site >> Stomach Cancer
Gene >> PDCD4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280154 |
| Start | 110887833:110887833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.724A>G |
| AA Mutation | p.Lys242Glu(p.K242E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280154 |
| Start | 110876055:110876055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.28A>G |
| AA Mutation | p.Asn10Asp(p.N10D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280154 |
| Start | 110881361:110881361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.172A>G |
| AA Mutation | p.Lys58Glu(p.K58E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280154 |
| Start | 110881358:110881358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.169G>A |
| AA Mutation | p.Ala57Thr(p.A57T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280154 |
| Start | 110887713:110887713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.604G>A |
| AA Mutation | p.Val202Met(p.V202M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280154 |
| Start | 110881438:110881438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538533354 |
| CDS Mutation | c.249C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |