Primary Site >> Esophagus Cancer
Gene >> RNF111
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000557998 |
| Start | 59066900:59066900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1503T>G |
| AA Mutation | p.His501Gln(p.H501Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000557998 |
| Start | 59080963:59080963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1976A>G |
| AA Mutation | p.His659Arg(p.H659R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000557998 |
| Start | 59091099:59091099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745792578 |
| CDS Mutation | c.2684G>A |
| AA Mutation | p.Arg895His(p.R895H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000557998 |
| Start | 59091149:59091149(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2738delA |
| AA Mutation | p.Lys913ArgfsTer2(p.K913Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000557998 |
| Start | 59081070:59081070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779592066 |
| CDS Mutation | c.2083C>T |
| AA Mutation | p.Gln695Ter(p.Q695*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000557998 |
| Start | 59076194:59076194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1927C>T |
| AA Mutation | p.Arg643Ter(p.R643*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |