Primary Site >> Liver Cancer
Gene >> NLRP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247436035:247436035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2564A>G |
| AA Mutation | p.His855Arg(p.H855R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247425395:247425395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1952C>A |
| AA Mutation | p.Pro651His(p.P651H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247424086:247424086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.643C>A |
| AA Mutation | p.His215Asn(p.H215N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247419062:247419062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.268G>T |
| AA Mutation | p.Asp90Tyr(p.D90Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247429718:247429718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2290A>G |
| AA Mutation | p.Thr764Ala(p.T764A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247424074:247424074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.631C>A |
| AA Mutation | p.Pro211Thr(p.P211T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247424927:247424927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768582957 |
| CDS Mutation | c.1484A>G |
| AA Mutation | p.Gln495Arg(p.Q495R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336119 |
| Start | 247444047:247444047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201764635 |
| CDS Mutation | c.2745G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336119 |
| Start | 247425393:247425393(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1953delC |
| AA Mutation | p.Lys652ArgfsTer70(p.K652Rfs*70) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |