single nucleotide variant | NM_024426.6(WT1):c.478C>T (p.Gln160Ter) | WT1 | Pathogenic | 11 | 32456429 | 32456429 | G | A | criteria provided, single submitter | ClinGen:CA379964944 |
single nucleotide variant | NM_024426.6(WT1):c.512G>T (p.Gly171Val) | WT1 | Likely pathogenic | 11 | 32456395 | 32456395 | C | A | criteria provided, single submitter | ClinGen:CA379964820 |
Deletion | NM_024426.6(WT1):c.543_556del (p.Tyr182fs) | WT1 | Pathogenic | 11 | 32456351 | 32456364 | CCGAAGGGCCCGTAG | C | criteria provided, single submitter | ClinGen:CA658658039 |
Deletion | NM_024426.6(WT1):c.653del (p.Arg218fs) | WT1 | Pathogenic | 11 | 32456254 | 32456254 | GC | G | criteria provided, single submitter | - |
Duplication | NM_024426.6(WT1):c.682dup (p.Asp228fs) | WT1 | Pathogenic | 11 | 32450144 | 32450145 | T | TC | criteria provided, single submitter | ClinGen:CA658658038 |
single nucleotide variant | NM_024426.6(WT1):c.699C>A (p.Tyr233Ter) | WT1 | Likely pathogenic | 11 | 32450128 | 32450128 | G | T | criteria provided, single submitter | ClinGen:CA379963503 |
Deletion | NM_024426.6(WT1):c.812del (p.Pro271fs) | WT1 | Pathogenic | 11 | 32449577 | 32449577 | CG | C | criteria provided, single submitter | ClinGen:CA16613560 |
single nucleotide variant | NM_024426.6(WT1):c.882C>A (p.Tyr294Ter) | WT1 | Pathogenic | 11 | 32449507 | 32449507 | G | T | criteria provided, single submitter | - |
Deletion | NC_000011.10:g.(?_32396251)_(32417660_?)del | WT1 | Pathogenic | 11 | 32417797 | 32439206 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_024426.6(WT1):c.965+1G>A | WT1 | Pathogenic/Likely pathogenic | 11 | 32439122 | 32439122 | C | T | criteria provided, multiple submitters, no conflicts | - |