Primary Site >> Pancreatic Cancer
Gene >> CHD7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60850552:60850552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5464G>A |
| AA Mutation | p.Gly1822Ser(p.G1822S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60822078:60822078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2890A>C |
| AA Mutation | p.Asn964His(p.N964H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60836225:60836225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3931A>G |
| AA Mutation | p.Ile1311Val(p.I1311V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60837765:60837765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4283C>A |
| AA Mutation | p.Ala1428Asp(p.A1428D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60856152:60856152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7114G>T |
| AA Mutation | p.Ala2372Ser(p.A2372S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000423902 |
| Start | 60854431:60854432(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.6847dupA |
| AA Mutation | p.Thr2283AsnfsTer20(p.T2283Nfs*20) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |