Primary Site >> Pancreatic Cancer
Gene >> NOS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151001897:151001897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757144684 |
| CDS Mutation | c.1579G>A |
| AA Mutation | p.Glu527Lys(p.E527K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151001945:151001945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762597577 |
| CDS Mutation | c.1627C>T |
| AA Mutation | p.Arg543Trp(p.R543W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 150995252:150995252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772393632 |
| CDS Mutation | c.208C>T |
| AA Mutation | p.Arg70Cys(p.R70C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151007264:151007264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2100G>T |
| AA Mutation | p.Gln700His(p.Q700H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151013238:151013238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3114G>T |
| AA Mutation | p.Gln1038His(p.Q1038H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297494 |
| Start | 151001600:151001600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1485C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |