single nucleotide variant | NM_000133.3(F9):c.-35G>A | F9 | Pathogenic | X | 138612889 | 138612889 | G | A | criteria provided, single submitter | OMIM:300746.0002,OMIM:300746.0003 |
Deletion | NC_000023.10:g.(?_138612860)_(139587225_?)del | F9 | Pathogenic | X | 138612860 | 139587225 | na | na | criteria provided, single submitter | - |
Deletion | NC_000023.11:g.(?_139530701)_(139563439_?)del | F9 | Pathogenic | X | 138612860 | 138645598 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_000133.4(F9):c.88G>A (p.Val30Ile) | F9 | Pathogenic | X | 138613011 | 138613011 | G | A | criteria provided, single submitter | - |
Deletion | NM_000133.4(F9):c.521-35_723+84del | F9 | Pathogenic | X | 138633185 | 138633506 | AAATATCAGGTTACTAATTTTTCTTCTATTTTTCTAGTGCCATTTCCATGTGGAAGAGTTTCTGTTTCACAAACTTCTAAGCTCACCCGTGCTGAGACTGTTTTTCCTGATGTGGACTATGTAAATTCTACTGAAGCTGAAACCATTTTGGATAACATCACTCAAAGCACCCAATCATTTAATGACTTCACTCGGGTTGTTGGTGGAGAAGATGCCAAACCAGGTCAATTCCCTTGGCAGGTACTTTATACTGATGGTGTGTCAAAACTGGAGCTCAGCTGGCAAGACACAGGCCAGGTGGGAGACTGAGGCTATTTTACTAG | A | criteria provided, single submitter | - |
Deletion | NM_000133.4(F9):c.724-5_731del | F9 | Likely pathogenic | X | 138642888 | 138642900 | TTTGTTTTCACAGG | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000133.4(F9):c.88+5G>T | F9 | Likely pathogenic | X | 138613016 | 138613016 | G | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000133.4(F9):c.88+1G>A | F9 | Likely pathogenic | X | 138613012 | 138613012 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000133.4(F9):c.*1157A>G | F9 | Pathogenic/Likely pathogenic | X | 138645387 | 138645387 | A | G | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000133.4(F9):c.1106T>C (p.Leu369Pro) | F9 | Likely pathogenic | X | 138643950 | 138643950 | T | C | criteria provided, multiple submitters, no conflicts | - |