Primary Site >> Stomach Cancer
Gene >> PRPF19
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227524 |
| Start | 60898147:60898147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1265G>A |
| AA Mutation | p.Arg422His(p.R422H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227524 |
| Start | 60899181:60899181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.952G>A |
| AA Mutation | p.Gly318Ser(p.G318S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227524 |
| Start | 60898183:60898183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1229C>T |
| AA Mutation | p.Ala410Val(p.A410V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227524 |
| Start | 60898621:60898621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060A>G |
| AA Mutation | p.Thr354Ala(p.T354A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227524 |
| Start | 60902745:60902745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.383G>A |
| AA Mutation | p.Arg128Gln(p.R128Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227524 |
| Start | 60898595:60898595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1086A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227524 |
| Start | 60900876:60900876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759269639 |
| CDS Mutation | c.696C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227524 |
| Start | 60903489:60903489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774634222 |
| CDS Mutation | c.216G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000227524 |
| Start | 60899281:60899281(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.852delC |
| AA Mutation | p.Asp285MetfsTer25(p.D285Mfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |