Primary Site >> Liver Cancer
Gene >> RASA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114018912:114018912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.793C>A |
| AA Mutation | p.Leu265Ile(p.L265I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114013148:114013148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1506C>A |
| AA Mutation | p.His502Gln(p.H502Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 114024282:114024282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.677T>A |
| AA Mutation | p.Ile226Asn(p.I226N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334062 |
| Start | 113981843:113981843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2261A>C |
| AA Mutation | p.Lys754Thr(p.K754T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334062 |
| Start | 114000842:114000842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1833C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334062 |
| Start | 114027870:114027870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141276378 |
| CDS Mutation | c.507C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |