Primary Site >> Liver Cancer
Gene >> HIPK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716875:139716875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.160A>T |
| AA Mutation | p.Ser54Cys(p.S54C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716876:139716876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.159G>T |
| AA Mutation | p.Gln53His(p.Q53H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139573385:139573385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3139A>G |
| AA Mutation | p.Ile1047Val(p.I1047V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139596865:139596865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2569T>A |
| AA Mutation | p.Cys857Ser(p.C857S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139600552:139600552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2300A>T |
| AA Mutation | p.Gln767Leu(p.Q767L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406875 |
| Start | 139716820:139716820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748732904 |
| CDS Mutation | c.215C>T |
| AA Mutation | p.Pro72Leu(p.P72L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000406875 |
| Start | 139631675:139631675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1154G>A |
| AA Mutation | p.Trp385Ter(p.W385*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000406875 |
| Start | 139572969:139572969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3555C>A |
| AA Mutation | p.Tyr1185Ter(p.Y1185*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000406875 |
| Start | 139626674:139626679(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1541_1546delAGAGAA |
| AA Mutation | p.Lys514_Arg515del(p.K514_R515del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |