Primary Site >> Liver Cancer
Gene >> NLRP5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56027481:56027481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1248G>T |
| AA Mutation | p.Lys416Asn(p.K416N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56004027:56004027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.374C>T |
| AA Mutation | p.Thr125Met(p.T125M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56033684:56033684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2590C>A |
| AA Mutation | p.Pro864Thr(p.P864T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56053664:56053664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778328871 |
| CDS Mutation | c.3155C>T |
| AA Mutation | p.Ala1052Val(p.A1052V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390649 |
| Start | 56027866:56027866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775936118 |
| CDS Mutation | c.1633G>T |
| AA Mutation | p.Val545Leu(p.V545L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390649 |
| Start | 56028165:56028165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776601668 |
| CDS Mutation | c.1932C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |