Primary Site >> Pancreatic Cancer
Gene >> NLRP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247418843:247418843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.49C>A |
| AA Mutation | p.Leu17Met(p.L17M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247424833:247424833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762512734 |
| CDS Mutation | c.1390G>A |
| AA Mutation | p.Ala464Thr(p.A464T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247425170:247425170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1727T>C |
| AA Mutation | p.Val576Ala(p.V576A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247434162:247434162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2387G>A |
| AA Mutation | p.Ser796Asn(p.S796N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247448470:247448470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3077C>A |
| AA Mutation | p.Pro1026His(p.P1026H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336119 |
| Start | 247424314:247424314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145092553 |
| CDS Mutation | c.871G>A |
| AA Mutation | p.Val291Met(p.V291M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336119 |
| Start | 247429687:247429687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2259G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |