Primary Site >> Stomach Cancer
Gene >> PRPF31
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321030 |
| Start | 54129069:54129069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1159G>A |
| AA Mutation | p.Ala387Thr(p.A387T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321030 |
| Start | 54131406:54131406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1474G>A |
| AA Mutation | p.Glu492Lys(p.E492K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321030 |
| Start | 54123816:54123816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142874574 |
| CDS Mutation | c.595G>A |
| AA Mutation | p.Ala199Thr(p.A199T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321030 |
| Start | 54118296:54118296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772745878 |
| CDS Mutation | c.18G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321030 |
| Start | 54123537:54123537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.504C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321030 |
| Start | 54121879:54121879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750573765 |
| CDS Mutation | c.258C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |