single nucleotide variant | NM_000132.4(F8):c.5954G>A (p.Arg1985Gln) | F8 | Pathogenic/Likely pathogenic | X | 154132225 | 154132225 | C | T | criteria provided, multiple submitters, no conflicts | - |
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_000132.4(F8):c.6547A>G (p.Met2183Val) | F8 | Pathogenic/Likely pathogenic | X | 154091385 | 154091385 | T | C | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000132.4(F8):c.1804C>G (p.Arg602Gly) | F8 | Pathogenic/Likely pathogenic | X | 154182266 | 154182266 | G | C | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000132.4(F8):c.979C>G (p.Leu327Val) | F8 | Pathogenic/Likely pathogenic | X | 154197636 | 154197636 | G | C | criteria provided, multiple submitters, no conflicts | - |
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 | - |