Primary Site >> Liver Cancer
Gene >> CADPS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62481850:62481850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3046C>A |
| AA Mutation | p.Pro1016Thr(p.P1016T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62536515:62536515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2033A>T |
| AA Mutation | p.His678Leu(p.H678L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62536516:62536516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2032C>A |
| AA Mutation | p.His678Asn(p.H678N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62645752:62645752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1295A>G |
| AA Mutation | p.Gln432Arg(p.Q432R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62481736:62481736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780894973 |
| CDS Mutation | c.3160A>T |
| AA Mutation | p.Ile1054Leu(p.I1054L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62874777:62874777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.253G>A |
| AA Mutation | p.Gly85Ser(p.G85S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62499209:62499209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2659G>A |
| AA Mutation | p.Glu887Lys(p.E887K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62874628:62874628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.402T>G |
| AA Mutation | p.Asn134Lys(p.N134K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62753445:62753445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.884G>C |
| AA Mutation | p.Cys295Ser(p.C295S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383710 |
| Start | 62874750:62874750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.280C>G |
| AA Mutation | p.Pro94Ala(p.P94A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383710 |
| Start | 62481752:62481752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368961255 |
| CDS Mutation | c.3144G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |