Primary Site >> Pancreatic Cancer
Gene >> NOS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117225040:117225040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3802C>T |
| AA Mutation | p.Arg1268Trp(p.R1268W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117265488:117265488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1964A>G |
| AA Mutation | p.Asp655Gly(p.D655G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117330709:117330709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.361C>T |
| AA Mutation | p.Arg121Trp(p.R121W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117330507:117330507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374847966 |
| CDS Mutation | c.563C>T |
| AA Mutation | p.Ala188Val(p.A188V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117265437:117265437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764344401 |
| CDS Mutation | c.2015G>A |
| AA Mutation | p.Arg672His(p.R672H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117290368:117290368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.911G>A |
| AA Mutation | p.Arg304His(p.R304H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117225039:117225039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3803G>A |
| AA Mutation | p.Arg1268Gln(p.R1268Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |