Primary Site >> Stomach Cancer
Gene >> ANKRD36C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000456556 |
| Start | 95980735:95980735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.644T>C |
| AA Mutation | p.Leu215Pro(p.L215P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000456556 |
| Start | 95891713:95891713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577035671 |
| CDS Mutation | c.2809G>C |
| AA Mutation | p.Val937Leu(p.V937L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000456556 |
| Start | 95927268:95927268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1885G>A |
| AA Mutation | p.Asp629Asn(p.D629N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000456556 |
| Start | 95857397:95857397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3992G>A |
| AA Mutation | p.Arg1331Lys(p.R1331K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000456556 |
| Start | 95991692:95991692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17C>A |
| AA Mutation | p.Pro6Gln(p.P6Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000456556 |
| Start | 95991561:95991561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.148T>G |
| AA Mutation | p.Phe50Val(p.F50V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000456556 |
| Start | 95991550:95991550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769954979 |
| CDS Mutation | c.159C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000456556 |
| Start | 95986790:95986790(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.447delA |
| AA Mutation | p.Lys149AsnfsTer24(p.K149Nfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |