Primary Site >> Pancreatic Cancer
Gene >> SIPA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641463:65641463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.542C>T |
| AA Mutation | p.Ala181Val(p.A181V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65649405:65649405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2450G>T |
| AA Mutation | p.Ser817Ile(p.S817I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394224 |
| Start | 65649441:65649441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2486C>A |
| AA Mutation | p.Thr829Asn(p.T829N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641494:65641494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764727662 |
| CDS Mutation | c.573C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641254:65641254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.333T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641428:65641428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.507C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394224 |
| Start | 65641497:65641497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750458317 |
| CDS Mutation | c.576G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |