Primary Site >> Liver Cancer
Gene >> DEPDC5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400246 |
| Start | 31838749:31838749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2419C>T |
| AA Mutation | p.Leu807Phe(p.L807F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400246 |
| Start | 31870729:31870729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3470A>C |
| AA Mutation | p.Asn1157Thr(p.N1157T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400246 |
| Start | 31845122:31845122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2906A>G |
| AA Mutation | p.Tyr969Cys(p.Y969C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400246 |
| Start | 31897540:31897540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4262A>T |
| AA Mutation | p.Glu1421Val(p.E1421V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400246 |
| Start | 31906459:31906459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4774A>G |
| AA Mutation | p.Thr1592Ala(p.T1592A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400246 |
| Start | 31819197:31819197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1842A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000400246 |
| Start | 31792777:31792777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772872014 |
| CDS Mutation | c.727C>T |
| AA Mutation | p.Arg243Ter(p.R243*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000400246 |
| Start | 31797669:31797670(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.843_844insTCAGTAT |
| AA Mutation | p.Pro282SerfsTer19(p.P282Sfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |