Primary Site >> Liver Cancer
Gene >> CCDC178
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383096 |
| Start | 33224905:33224905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1688C>A |
| AA Mutation | p.Ala563Glu(p.A563E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383096 |
| Start | 32974635:32974635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2435T>A |
| AA Mutation | p.Phe812Tyr(p.F812Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383096 |
| Start | 33092768:33092768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2381A>T |
| AA Mutation | p.Lys794Met(p.K794M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383096 |
| Start | 33267253:33267253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1221A>C |
| AA Mutation | p.Gln407His(p.Q407H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383096 |
| Start | 32974671:32974671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2399T>A |
| AA Mutation | p.Leu800Gln(p.L800Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383096 |
| Start | 33333368:33333368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.685A>T |
| AA Mutation | p.Ile229Leu(p.I229L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383096 |
| Start | 33266976:33266976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371081933 |
| CDS Mutation | c.1349C>T |
| AA Mutation | p.Thr450Met(p.T450M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383096 |
| Start | 33215688:33215688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776180170 |
| CDS Mutation | c.1940G>T |
| AA Mutation | p.Arg647Leu(p.R647L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383096 |
| Start | 33346251:33346251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.618A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |