Primary Site >> Pancreatic Cancer
Gene >> RICTOR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38942876:38942876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5009G>A |
| AA Mutation | p.Arg1670Gln(p.R1670Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38947434:38947434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4144A>C |
| AA Mutation | p.Lys1382Gln(p.K1382Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38949902:38949902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3946G>A |
| AA Mutation | p.Asp1316Asn(p.D1316N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38950183:38950183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3665C>T |
| AA Mutation | p.Thr1222Ile(p.T1222I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38953034:38953034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2848C>T |
| AA Mutation | p.Pro950Ser(p.P950S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38954797:38954797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2674G>A |
| AA Mutation | p.Gly892Ser(p.G892S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |