Deletion | NC_000011.10:g.(?_32389048)_(32435355_?)del | WT1 | Pathogenic | 11 | 32410594 | 32456901 | na | na | criteria provided, single submitter | - |
Deletion | NC_000011.10:g.(?_32389058)_(32435345_?)del | WT1 | Pathogenic | 11 | 32410604 | 32456891 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_024426.6(WT1):c.1499G>A (p.Arg500Gln) | WT1 | Pathogenic | 11 | 32410674 | 32410674 | C | T | criteria provided, single submitter | - |
single nucleotide variant | NM_024426.6(WT1):c.1447+5G>A | WT1 | Pathogenic | 11 | 32413513 | 32413513 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA016607,OMIM:607102.0009,OMIM:607102.0020 |
single nucleotide variant | NM_024426.6(WT1):c.1447+4C>T | WT1 | Pathogenic/Likely pathogenic | 11 | 32413514 | 32413514 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA016600,OMIM:607102.0018 |
single nucleotide variant | NM_024426.6(WT1):c.1421A>C (p.His474Pro) | WT1 | Likely pathogenic | 11 | 32413544 | 32413544 | T | G | criteria provided, single submitter | - |
single nucleotide variant | NM_024426.6(WT1):c.1406A>G (p.Asp469Gly) | WT1 | Likely pathogenic | 11 | 32413559 | 32413559 | T | C | criteria provided, single submitter | ClinGen:CA016344,OMIM:607102.0005 |
single nucleotide variant | NM_024426.6(WT1):c.1405G>A (p.Asp469Asn) | WT1 | Pathogenic | 11 | 32413560 | 32413560 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA016338,OMIM:607102.0006 |
single nucleotide variant | NM_024426.6(WT1):c.1405G>T (p.Asp469Tyr) | WT1 | Pathogenic/Likely pathogenic | 11 | 32413560 | 32413560 | C | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_024426.6(WT1):c.1400G>C (p.Arg467Pro) | WT1 | Pathogenic | 11 | 32413565 | 32413565 | C | G | criteria provided, single submitter | ClinGen:CA016330,OMIM:607102.0007 |