Primary Site >> Liver Cancer
Gene >> NOS3
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000297494 |
| Start | 151010986:151010986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2984G>C |
| AA Mutation | p.Gly995Ala(p.G995A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 150999227:150999227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749115207 |
| CDS Mutation | c.994G>A |
| AA Mutation | p.Ala332Thr(p.A332T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 150998584:150998584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.720C>A |
| AA Mutation | p.Asp240Glu(p.D240E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 150998360:150998360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.586T>G |
| AA Mutation | p.Phe196Val(p.F196V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151001293:151001293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145811781 |
| CDS Mutation | c.1296G>T |
| AA Mutation | p.Glu432Asp(p.E432D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 150999227:150999227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.994G>C |
| AA Mutation | p.Ala332Pro(p.A332P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297494 |
| Start | 151001263:151001263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534664057 |
| CDS Mutation | c.1266C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297494 |
| Start | 151013310:151013317(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3186_3193delGAACGCCC |
| AA Mutation | p.Asn1063AlafsTer17(p.N1063Afs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |