single nucleotide variant | NM_005633.4(SOS1):c.2536G>A (p.Glu846Lys) | SOS1 | Pathogenic | 2 | 39234309 | 39234309 | C | T | reviewed by expert panel | ClinGen:CA261734,UniProtKB:Q07889#VAR_030441 |
single nucleotide variant | NM_005633.4(SOS1):c.2197A>T (p.Ile733Phe) | SOS1 | Pathogenic/Likely pathogenic | 2 | 39239460 | 39239460 | T | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA297205,UniProtKB:Q07889#VAR_030440 |
single nucleotide variant | NM_005633.4(SOS1):c.2183A>T (p.Lys728Ile) | SOS1 | Pathogenic/Likely pathogenic | 2 | 39239474 | 39239474 | T | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA261731 |
single nucleotide variant | NM_005633.4(SOS1):c.2104T>C (p.Tyr702His) | SOS1 | Pathogenic | 2 | 39240664 | 39240664 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA273696,UniProtKB:Q07889#VAR_030438 |
single nucleotide variant | NM_005633.4(SOS1):c.1656G>T (p.Arg552Ser) | SOS1 | Pathogenic | 2 | 39249913 | 39249913 | C | A | reviewed by expert panel | ClinGen:CA261730,UniProtKB:Q07889#VAR_030436,LOVD 3:SOS1_000053,OMIM:182530.0005 |
single nucleotide variant | NM_005633.4(SOS1):c.1655G>A (p.Arg552Lys) | SOS1 | Pathogenic | 2 | 39249914 | 39249914 | C | T | reviewed by expert panel | ClinGen:CA261726,UniProtKB:Q07889#VAR_030435 |
single nucleotide variant | NM_005633.4(SOS1):c.1655G>C (p.Arg552Thr) | SOS1 | Pathogenic | 2 | 39249914 | 39249914 | C | G | reviewed by expert panel | ClinGen:CA261728,UniProtKB:Q07889#VAR_066049 |
single nucleotide variant | NM_005633.4(SOS1):c.1655G>T (p.Arg552Met) | SOS1 | Likely pathogenic | 2 | 39249914 | 39249914 | C | A | reviewed by expert panel | ClinGen:CA16616762 |
single nucleotide variant | NM_005633.4(SOS1):c.1649T>C (p.Leu550Pro) | SOS1 | Pathogenic | 2 | 39249920 | 39249920 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA261724,UniProtKB:Q07889#VAR_030433 |
single nucleotide variant | NM_005633.4(SOS1):c.1644T>A (p.Ser548Arg) | SOS1 | Pathogenic | 2 | 39249925 | 39249925 | A | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA297272,UniProtKB:Q07889#VAR_030432 |