single nucleotide variant | NM_000130.5(F5):c.6304C>T (p.Arg2102Cys) | F5 | Likely pathogenic | 1 | 169487691 | 169487691 | G | A | criteria provided, single submitter | ClinGen:CA251559,UniProtKB:P12259#VAR_032701,OMIM:612309.0012 |
single nucleotide variant | NM_000130.5(F5):c.2218C>T (p.Arg740Ter) | F5 | Likely pathogenic | 1 | 169512110 | 169512110 | G | A | criteria provided, single submitter | ClinGen:CA10608192 |
Duplication | NM_000130.5(F5):c.5403dup (p.Ser1802fs) | F5 | Likely pathogenic | 1 | 169498861 | 169498862 | A | AT | criteria provided, single submitter | ClinGen:CA1233514 |
Deletion | NM_000130.5(F5):c.3170_3174del (p.Asn1057fs) | F5 | Likely pathogenic | 1 | 169511154 | 169511158 | ATGTGT | A | criteria provided, single submitter | - |
Deletion | NM_000130.5(F5):c.2862del (p.Ser955fs) | F5 | Likely pathogenic | 1 | 169511466 | 169511466 | TA | T | criteria provided, single submitter | OMIM:612309.0010 |
Deletion | NM_000130.5(F5):c.2539del (p.Ile847fs) | F5 | Likely pathogenic | 1 | 169511789 | 169511789 | AT | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000130.5(F5):c.1671G>C (p.Trp557Cys) | F5 | Likely pathogenic | 1 | 169515771 | 169515771 | C | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000130.5(F5):c.1498T>G (p.Cys500Gly) | F5 | Likely pathogenic | 1 | 169519152 | 169519152 | A | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000130.5(F5):c.1297-2A>G | F5 | Likely pathogenic | 1 | 169519979 | 169519979 | T | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000130.5(F5):c.1674C>A (p.Tyr558Ter) | F5 | Likely pathogenic | 1 | 169515768 | 169515768 | G | T | criteria provided, single submitter | - |