Primary Site >> Liver Cancer
Gene >> EPHA5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273854 |
| Start | 65602153:65602153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.398C>T |
| AA Mutation | p.Thr133Ile(p.T133I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273854 |
| Start | 65490697:65490697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1082C>G |
| AA Mutation | p.Pro361Arg(p.P361R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273854 |
| Start | 65601661:65601661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.890A>T |
| AA Mutation | p.Glu297Val(p.E297V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273854 |
| Start | 65602217:65602217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.334T>A |
| AA Mutation | p.Trp112Arg(p.W112R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273854 |
| Start | 65353065:65353065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2275G>A |
| AA Mutation | p.Gly759Ser(p.G759S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273854 |
| Start | 65414349:65414349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1622G>A |
| AA Mutation | p.Arg541Gln(p.R541Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273854 |
| Start | 65495506:65495506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.948C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273854 |
| Start | 65602173:65602173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs55882537 |
| CDS Mutation | c.378C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |