Primary Site >> Liver Cancer
Gene >> SOS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402219 |
| Start | 39022786:39022786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642A>G |
| AA Mutation | p.Ser548Gly(p.S548G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402219 |
| Start | 39051265:39051265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775052125 |
| CDS Mutation | c.743G>A |
| AA Mutation | p.Arg248His(p.R248H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402219 |
| Start | 39012237:39012237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs730881027 |
| CDS Mutation | c.2279C>T |
| AA Mutation | p.Thr760Ile(p.T760I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402219 |
| Start | 39023089:39023089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1339G>A |
| AA Mutation | p.Glu447Lys(p.E447K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402219 |
| Start | 38995293:38995293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767619216 |
| CDS Mutation | c.3176A>G |
| AA Mutation | p.Glu1059Gly(p.E1059G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402219 |
| Start | 39023128:39023128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397517148 |
| CDS Mutation | c.1300G>A |
| AA Mutation | p.Gly434Arg(p.G434R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402219 |
| Start | 38985958:38985958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3868C>T |
| AA Mutation | p.Pro1290Ser(p.P1290S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |