Primary Site >> Liver Cancer
Gene >> NLRP12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810736:53810736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.923G>A |
| AA Mutation | p.Gly308Glu(p.G308E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810659:53810659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1000C>T |
| AA Mutation | p.Pro334Ser(p.P334S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53811241:53811241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.418A>T |
| AA Mutation | p.Met140Leu(p.M140L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53798385:53798385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146368839 |
| CDS Mutation | c.2785G>A |
| AA Mutation | p.Ala929Thr(p.A929T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53805328:53805328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2366T>C |
| AA Mutation | p.Leu789Pro(p.L789P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53807622:53807622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2116G>C |
| AA Mutation | p.Ala706Pro(p.A706P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53823902:53823902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.273A>T |
| AA Mutation | p.Arg91Ser(p.R91S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324134 |
| Start | 53803980:53803980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2557C>A |
| AA Mutation | p.His853Asn(p.H853N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810033:53810033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753966022 |
| CDS Mutation | c.1626C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324134 |
| Start | 53810965:53810965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.694C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |