ClinVar Miner

List of variants in gene SOS1 reported as likely benign by Invitae

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Total variants: 20
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HGVS dbSNP
NM_005633.3(SOS1):c.109A>G (p.Thr37Ala) rs150565592
NM_005633.3(SOS1):c.1191A>G (p.Lys397=) rs770175415
NM_005633.3(SOS1):c.1648C>T (p.Leu550=) rs1233000238
NM_005633.3(SOS1):c.214-10A>G rs371447614
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.3(SOS1):c.2674-9dup rs532594344
NM_005633.3(SOS1):c.273A>G (p.Gln91=) rs914110575
NM_005633.3(SOS1):c.2791+7_2791+10delATTT rs760707217
NM_005633.3(SOS1):c.3032A>G (p.Asn1011Ser) rs8192671
NM_005633.3(SOS1):c.3060C>T (p.Asn1020=) rs142431345
NM_005633.3(SOS1):c.3330G>C (p.Ser1110=) rs146383828
NM_005633.3(SOS1):c.3813G>A (p.Arg1271=) rs863224405
NM_005633.3(SOS1):c.39A>G (p.Glu13=) rs763337946
NM_005633.3(SOS1):c.511-9_511-6delACTG rs986512473
NM_005633.3(SOS1):c.543A>G (p.Glu181=) rs201068374
NM_005633.3(SOS1):c.582C>T (p.Ser194=) rs746685895
NM_005633.3(SOS1):c.675T>G (p.Val225=) rs371482290
NM_005633.3(SOS1):c.720+9C>T rs370687707
NM_005633.3(SOS1):c.73C>T (p.Pro25Ser) rs139592595
NM_005633.3(SOS1):c.749T>C (p.Val250Ala) rs139290271

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