Primary Site >> Liver Cancer
Gene >> EPHA6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389672 |
| Start | 96987579:96987579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.700T>G |
| AA Mutation | p.Phe234Val(p.F234V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389672 |
| Start | 97532529:97532529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2372G>C |
| AA Mutation | p.Gly791Ala(p.G791A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389672 |
| Start | 97448638:97448638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1802C>A |
| AA Mutation | p.Pro601Gln(p.P601Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389672 |
| Start | 96987859:96987859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.980G>A |
| AA Mutation | p.Arg327Gln(p.R327Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389672 |
| Start | 97484039:97484039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2180T>C |
| AA Mutation | p.Ile727Thr(p.I727T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389672 |
| Start | 97226355:97226355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758462964 |
| CDS Mutation | c.1206T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389672 |
| Start | 97532530:97532530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2373G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389672 |
| Start | 97475401:97475401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372907476 |
| CDS Mutation | c.1944C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389672 |
| Start | 96987386:96987386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762684823 |
| CDS Mutation | c.507A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |