Primary Site >> Pancreatic Cancer
Gene >> NAV3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397909 |
| Start | 78007147:78007147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1609G>A |
| AA Mutation | p.Val537Ile(p.V537I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397909 |
| Start | 78116822:78116822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2687A>C |
| AA Mutation | p.Asn896Thr(p.N896T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397909 |
| Start | 78119326:78119326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3130A>G |
| AA Mutation | p.Ser1044Gly(p.S1044G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397909 |
| Start | 78210460:78210460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752366967 |
| CDS Mutation | c.7101C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397909 |
| Start | 78177284:78177284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5268A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397909 |
| Start | 78210430:78210430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7071C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000397909 |
| Start | 78190054:78190054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6126C>A |
| AA Mutation | p.Tyr2042Ter(p.Y2042*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |