Primary Site >> Pancreatic Cancer
Gene >> NOD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711226:50711226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375201229 |
| CDS Mutation | c.1315C>T |
| AA Mutation | p.Arg439Cys(p.R439C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711287:50711287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753458507 |
| CDS Mutation | c.1376G>A |
| AA Mutation | p.Arg459His(p.R459H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711581:50711581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1670G>A |
| AA Mutation | p.Gly557Asp(p.G557D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711975:50711975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2064C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300589 |
| Start | 50699702:50699702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.288T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300589 |
| Start | 50712110:50712110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2199G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |