Primary Site >> Pancreatic Cancer
Gene >> IFT122
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348417 |
| Start | 129481566:129481566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368750069 |
| CDS Mutation | c.1525G>A |
| AA Mutation | p.Val509Ile(p.V509I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348417 |
| Start | 129519648:129519648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3552G>T |
| AA Mutation | p.Lys1184Asn(p.K1184N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348417 |
| Start | 129519683:129519683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3587G>A |
| AA Mutation | p.Arg1196His(p.R1196H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348417 |
| Start | 129476738:129476738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765777740 |
| CDS Mutation | c.1084C>T |
| AA Mutation | p.Arg362Cys(p.R362C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348417 |
| Start | 129495586:129495586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2187C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348417 |
| Start | 129515574:129515574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3240C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |