Primary Site >> Liver Cancer
Gene >> EPHA10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373048 |
| Start | 37765026:37765026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.41T>A |
| AA Mutation | p.Leu14His(p.L14H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373048 |
| Start | 37761785:37761785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.470C>T |
| AA Mutation | p.Ala157Val(p.A157V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373048 |
| Start | 37719945:37719945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2526T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373048 |
| Start | 37731547:37731547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755623091 |
| CDS Mutation | c.1527A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373048 |
| Start | 37721712:37721712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2094G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373048 |
| Start | 37762003:37762003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.252G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |