Primary Site >> Liver Cancer
Gene >> ABCA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341511 |
| Start | 137008502:137008502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7189C>A |
| AA Mutation | p.Pro2397Thr(p.P2397T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341511 |
| Start | 137013506:137013506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755244581 |
| CDS Mutation | c.4505G>A |
| AA Mutation | p.Arg1502His(p.R1502H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341511 |
| Start | 137015756:137015756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3433A>G |
| AA Mutation | p.Ile1145Val(p.I1145V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341511 |
| Start | 137022368:137022368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367828133 |
| CDS Mutation | c.550C>T |
| AA Mutation | p.Arg184Cys(p.R184C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341511 |
| Start | 137010058:137010058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748279912 |
| CDS Mutation | c.6420C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341511 |
| Start | 137012308:137012308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5256G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |