single nucleotide variant | NM_000132.4(F8):c.877C>G (p.His293Asp) | F8 | Likely pathogenic | X | 154197738 | 154197738 | G | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.1952A>C (p.His651Pro) | F8 | Likely pathogenic | X | 154176134 | 154176134 | T | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.2161A>C (p.Met721Leu) | F8 | Likely pathogenic | X | 154159904 | 154159904 | T | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.5417C>T (p.Ser1806Phe) | F8 | Likely pathogenic | X | 154133255 | 154133255 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.5939A>G (p.His1980Arg) | F8 | Likely pathogenic | X | 154132240 | 154132240 | T | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.6278A>T (p.Asp2093Val) | F8 | Likely pathogenic | X | 154124503 | 154124503 | T | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.6320G>A (p.Gly2107Asp) | F8 | Likely pathogenic | X | 154124461 | 154124461 | C | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000132.4(F8):c.6967C>G (p.Arg2323Gly) | F8 | Likely pathogenic | X | 154065961 | 154065961 | G | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000133.4(F9):c.1289G>A (p.Ser430Asn) | F9 | Likely pathogenic | X | 138644133 | 138644133 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000133.4(F9):c.1256T>G (p.Val419Gly) | F9 | Likely pathogenic | X | 138644100 | 138644100 | T | G | criteria provided, single submitter | - |