Primary Site >> Liver Cancer
Gene >> NOS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27768998:27768998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2013C>A |
| AA Mutation | p.Ser671Arg(p.S671R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27762894:27762894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2704A>T |
| AA Mutation | p.Ile902Phe(p.I902F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27779009:27779009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1052C>T |
| AA Mutation | p.Ala351Val(p.A351V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27782981:27782981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.593C>T |
| AA Mutation | p.Pro198Leu(p.P198L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27761208:27761208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2824G>A |
| AA Mutation | p.Gly942Ser(p.G942S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313735 |
| Start | 27789611:27789611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141421929 |
| CDS Mutation | c.188C>T |
| AA Mutation | p.Thr63Met(p.T63M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313735 |
| Start | 27769570:27769570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759255233 |
| CDS Mutation | c.1824G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |