Primary Site >> Stomach Cancer
Gene >> ANKRD6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339746 |
| Start | 89630840:89630840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2020G>A |
| AA Mutation | p.Ala674Thr(p.A674T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339746 |
| Start | 89613837:89613837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.562T>C |
| AA Mutation | p.Ser188Pro(p.S188P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339746 |
| Start | 89627587:89627587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768555283 |
| CDS Mutation | c.1376G>A |
| AA Mutation | p.Arg459His(p.R459H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339746 |
| Start | 89616575:89616575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632T>G |
| AA Mutation | p.Leu211Arg(p.L211R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339746 |
| Start | 89566998:89566998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369619069 |
| CDS Mutation | c.22G>A |
| AA Mutation | p.Ala8Thr(p.A8T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339746 |
| Start | 89603082:89603082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780694454 |
| CDS Mutation | c.273C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339746 |
| Start | 89623964:89623964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1125C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339746 |
| Start | 89623982:89623982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1143C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000339746 |
| Start | 89627590:89627590(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1382delT |
| AA Mutation | p.Leu461TrpfsTer4(p.L461Wfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000339746 |
| Start | 89630830:89630830(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs757124885 |
| CDS Mutation | c.2016delT |
| AA Mutation | p.Phe672LeufsTer34(p.F672Lfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |