single nucleotide variant | NM_000132.4(F8):c.733C>T (p.Arg245Trp) | F8 | Pathogenic/Likely pathogenic | X | 154213016 | 154213016 | G | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000132.4(F8):c.558C>A (p.Asp186Glu) | F8 | Likely pathogenic | X | 154221254 | 154221254 | G | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.460A>C (p.Thr154Pro) | F8 | Likely pathogenic | X | 154221352 | 154221352 | T | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.143G>A (p.Arg48Lys) | F8 | Likely pathogenic | X | 154250685 | 154250685 | C | 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.88+5G>T | F9 | Likely pathogenic | X | 138613016 | 138613016 | G | T | 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_000132.4(F8):c.5219+2T>C | F8 | Likely pathogenic | X | 154156844 | 154156844 | A | G | 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 | - |
Complex | Single allele | F8 | Likely pathogenic | X | 154156796 | 154227925 | na | na | criteria provided, single submitter | - |