Primary Site >> Liver Cancer
Gene >> ANGPT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000517746 |
| Start | 107284815:107284815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1072G>T |
| AA Mutation | p.Gly358Trp(p.G358W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000517746 |
| Start | 107322122:107322122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.582A>T |
| AA Mutation | p.Leu194Phe(p.L194F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000517746 |
| Start | 107284738:107284738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1149C>G |
| AA Mutation | p.Asn383Lys(p.N383K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000517746 |
| Start | 107336203:107336203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.522G>C |
| AA Mutation | p.Glu174Asp(p.E174D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000517746 |
| Start | 107303346:107303346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.830G>T |
| AA Mutation | p.Arg277Ile(p.R277I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000517746 |
| Start | 107321957:107321957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138528651 |
| CDS Mutation | c.747G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |