Primary Site >> Liver Cancer
Gene >> RASA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274376 |
| Start | 87389504:87389504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3037A>G |
| AA Mutation | p.Ser1013Gly(p.S1013G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274376 |
| Start | 87372190:87372190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1771C>G |
| AA Mutation | p.Arg591Gly(p.R591G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274376 |
| Start | 87338050:87338050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.976G>A |
| AA Mutation | p.Asp326Asn(p.D326N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274376 |
| Start | 87376546:87376546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2165A>C |
| AA Mutation | p.Glu722Ala(p.E722A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274376 |
| Start | 87333302:87333302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777884338 |
| CDS Mutation | c.864A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274376 |
| Start | 87338049:87338049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.975A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000274376 |
| Start | 87376417:87376417(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2036delG |
| AA Mutation | p.Arg679HisfsTer20(p.R679Hfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000274376 |
| Start | 87369839:87369851(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1639_1651delCACTTTAGTGAAG |
| AA Mutation | p.His547AsnfsTer19(p.H547Nfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000274376 |
| Start | 87341317:87341317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1045A>T |
| AA Mutation | p.Lys349Ter(p.K349*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000274376 |
| Start | 87363376:87363376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1482T>G |
| AA Mutation | p.Tyr494Ter(p.Y494*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000274376 |
| Start | 87268740:87268760(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775227380 |
| CDS Mutation | c.299_319delCTGGCGTGGCCGGTGCTGCTG |
| AA Mutation | p.Ala100_Ala106del(p.A100_A106del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | start_lost |
| Transcription ID | ENST00000274376 |
| Start | 87268452:87268452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1A>G |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |