Primary Site >> Liver Cancer
Gene >> RPTOR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306801 |
| Start | 80730630:80730630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.578T>C |
| AA Mutation | p.Val193Ala(p.V193A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306801 |
| Start | 80957702:80957702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3449G>T |
| AA Mutation | p.Trp1150Leu(p.W1150L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306801 |
| Start | 80957703:80957703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3450G>T |
| AA Mutation | p.Trp1150Cys(p.W1150C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306801 |
| Start | 80730629:80730629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.577G>A |
| AA Mutation | p.Val193Ile(p.V193I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306801 |
| Start | 80883815:80883815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1685G>A |
| AA Mutation | p.Cys562Tyr(p.C562Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306801 |
| Start | 80945746:80945746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145803652 |
| CDS Mutation | c.3105G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306801 |
| Start | 80822282:80822282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375226529 |
| CDS Mutation | c.972G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306801 |
| Start | 80945749:80945749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3108G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |