Primary Site >> Pancreatic Cancer
Gene >> SBNO2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361757 |
| Start | 1109689:1109689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3117C>A |
| AA Mutation | p.Phe1039Leu(p.F1039L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361757 |
| Start | 1112482:1112482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2435G>A |
| AA Mutation | p.Arg812His(p.R812H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361757 |
| Start | 1112517:1112517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2400G>T |
| AA Mutation | p.Glu800Asp(p.E800D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361757 |
| Start | 1119097:1119097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1441C>A |
| AA Mutation | p.Leu481Ile(p.L481I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361757 |
| Start | 1119154:1119154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376023611 |
| CDS Mutation | c.1384G>A |
| AA Mutation | p.Ala462Thr(p.A462T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361757 |
| Start | 1109545:1109545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3177G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361757 |
| Start | 1112469:1112469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2448C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |