Primary Site >> Pancreatic Cancer
Gene >> BRCA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380152 |
| Start | 32332311:32332311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.833G>A |
| AA Mutation | p.Ser278Asn(p.S278N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380152 |
| Start | 32337404:32337404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3049A>T |
| AA Mutation | p.Ile1017Phe(p.I1017F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380152 |
| Start | 32338392:32338392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4037C>A |
| AA Mutation | p.Thr1346Asn(p.T1346N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380152 |
| Start | 32339280:32339280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80358718 |
| CDS Mutation | c.4925A>C |
| AA Mutation | p.Asn1642Thr(p.N1642T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380152 |
| Start | 32340590:32340590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6235G>A |
| AA Mutation | p.Val2079Met(p.V2079M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380152 |
| Start | 32379835:32379835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9039T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380152 |
| Start | 32363343:32363343(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.8145delA |
| AA Mutation | p.Val2716TrpfsTer17(p.V2716Wfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380152 |
| Start | 32339699:32339700(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.5351dupA |
| AA Mutation | p.Asn1784LysfsTer3(p.N1784Kfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |