Primary Site >> Liver Cancer
Gene >> DACH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613252 |
| Start | 71475198:71475198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2026C>A |
| AA Mutation | p.Pro676Thr(p.P676T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613252 |
| Start | 71630693:71630693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.989C>A |
| AA Mutation | p.Ala330Asp(p.A330D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613252 |
| Start | 71866205:71866205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.565A>G |
| AA Mutation | p.Lys189Glu(p.K189E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613252 |
| Start | 71475172:71475172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2052C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613252 |
| Start | 71489138:71489138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370706409 |
| CDS Mutation | c.1581G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | start_lost |
| Transcription ID | ENST00000613252 |
| Start | 71866769:71866769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1A>T |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |