ClinVar Miner

List of variants in gene SOS1 reported as likely pathogenic for not provided

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Gene type:
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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_005633.4(SOS1):c.1654A>T (p.Arg552Trp) rs137852814 0.00001
NM_005633.4(SOS1):c.2105A>G (p.Tyr702Cys) rs757094189 0.00001
NM_005633.4(SOS1):c.1276C>A (p.Gln426Lys) rs1558474706
NM_005633.4(SOS1):c.1285A>G (p.Ile429Val) rs2124537717
NM_005633.4(SOS1):c.1310T>C (p.Ile437Thr) rs397517150
NM_005633.4(SOS1):c.1316A>C (p.Gln439Pro) rs1057517861
NM_005633.4(SOS1):c.1355G>C (p.Arg452Pro)
NM_005633.4(SOS1):c.1433C>G (p.Pro478Arg) rs1553356111
NM_005633.4(SOS1):c.1646C>A (p.Thr549Lys) rs730881046
NM_005633.4(SOS1):c.1655G>T (p.Arg552Met) rs397517154
NM_005633.4(SOS1):c.1859A>G (p.Asp620Gly) rs1057517918
NM_005633.4(SOS1):c.2183A>T (p.Lys728Ile) rs397517156
NM_005633.4(SOS1):c.224A>T (p.Gln75Leu) rs786205522
NM_005633.4(SOS1):c.305C>G (p.Pro102Arg) rs1553362937
NM_005633.4(SOS1):c.323A>G (p.Glu108Gly) rs886041923
NM_005633.4(SOS1):c.323A>T (p.Glu108Val) rs886041923
NM_005633.4(SOS1):c.508A>G (p.Lys170Glu) rs397517172
NM_005633.4(SOS1):c.512T>C (p.Val171Ala) rs397517174

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