Primary Site >> Stomach Cancer
Gene >> NOS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151009209:151009209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2266C>T |
| AA Mutation | p.Arg756Trp(p.R756W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151014072:151014072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750442776 |
| CDS Mutation | c.3515G>A |
| AA Mutation | p.Arg1172His(p.R1172H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151010127:151010127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2525C>T |
| AA Mutation | p.Pro842Leu(p.P842L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151010124:151010124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760324893 |
| CDS Mutation | c.2522C>T |
| AA Mutation | p.Pro841Leu(p.P841L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151001577:151001577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1462A>G |
| AA Mutation | p.Thr488Ala(p.T488A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 150999022:150999022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.893A>C |
| AA Mutation | p.Asp298Ala(p.D298A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 150999281:150999281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376007167 |
| CDS Mutation | c.1048G>A |
| AA Mutation | p.Ala350Thr(p.A350T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151006903:151006903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1835G>A |
| AA Mutation | p.Arg612His(p.R612H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151014045:151014045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3488C>T |
| AA Mutation | p.Thr1163Met(p.T1163M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297494 |
| Start | 151014102:151014102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3545A>C |
| AA Mutation | p.Glu1182Ala(p.E1182A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297494 |
| Start | 150999319:150999319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1086C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297494 |
| Start | 151014037:151014037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297494 |
| Start | 151001310:151001310(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1319delG |
| AA Mutation | p.Gly440AlafsTer64(p.G440Afs*64) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297494 |
| Start | 151010123:151010123(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2526delC |
| AA Mutation | p.Gly843AlafsTer115(p.G843Afs*115) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297494 |
| Start | 151001309:151001310(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs749517498 |
| CDS Mutation | c.1319dupG |
| AA Mutation | p.Cys441LeufsTer57(p.C441Lfs*57) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |