Primary Site >> Stomach Cancer
Gene >> IFI44
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370747 |
| Start | 78655465:78655465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794A>C |
| AA Mutation | p.Asp265Ala(p.D265A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370747 |
| Start | 78655127:78655127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.608T>C |
| AA Mutation | p.Phe203Ser(p.F203S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370747 |
| Start | 78662735:78662735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1145C>A |
| AA Mutation | p.Ala382Asp(p.A382D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370747 |
| Start | 78655038:78655038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.519C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370747 |
| Start | 78663802:78663802(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1332delA |
| AA Mutation | p.Lys444AsnfsTer17(p.K444Nfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000370747 |
| Start | 78659462:78659462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780475679 |
| CDS Mutation | c.991C>T |
| AA Mutation | p.Arg331Ter(p.R331*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |