Primary Site >> Stomach Cancer
Gene >> NFIL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297689 |
| Start | 91410666:91410666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.69C>A |
| AA Mutation | p.Asp23Glu(p.D23E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297689 |
| Start | 91409605:91409605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1130C>T |
| AA Mutation | p.Ser377Phe(p.S377F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297689 |
| Start | 91409915:91409915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.820A>G |
| AA Mutation | p.Thr274Ala(p.T274A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297689 |
| Start | 91410144:91410144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.591A>C |
| AA Mutation | p.Glu197Asp(p.E197D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297689 |
| Start | 91409822:91409822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.913C>G |
| AA Mutation | p.Leu305Val(p.L305V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297689 |
| Start | 91410502:91410502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.233A>G |
| AA Mutation | p.Glu78Gly(p.E78G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297689 |
| Start | 91410243:91410243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766517635 |
| CDS Mutation | c.492C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |