ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP
NM_005633.3(SOS1):c.1095A>G (p.Glu365=) rs767540464
NM_005633.3(SOS1):c.109A>G (p.Thr37Ala) rs150565592
NM_005633.3(SOS1):c.1134A>G (p.Thr378=) rs1572831555
NM_005633.3(SOS1):c.1191A>G (p.Lys397=) rs770175415
NM_005633.3(SOS1):c.1198C>T (p.Leu400=) rs1572831511
NM_005633.3(SOS1):c.1251A>C (p.Leu417=) rs144027132
NM_005633.3(SOS1):c.1344A>C (p.Gly448=) rs981794978
NM_005633.3(SOS1):c.1554A>G (p.Leu518=) rs765369803
NM_005633.3(SOS1):c.1648C>T (p.Leu550=) rs1233000238
NM_005633.3(SOS1):c.1772A>G (p.Asn591Ser) rs757213444
NM_005633.3(SOS1):c.1854C>T (p.Tyr618=) rs727505181
NM_005633.3(SOS1):c.1905C>T (p.Cys635=) rs762900789
NM_005633.3(SOS1):c.1953A>G (p.Pro651=) rs141507912
NM_005633.3(SOS1):c.1962G>A (p.Glu654=) rs144382701
NM_005633.3(SOS1):c.2010G>C (p.Leu670Phe) rs200712930
NM_005633.3(SOS1):c.214-10A>G rs371447614
NM_005633.3(SOS1):c.2167+8T>C rs1422066325
NM_005633.3(SOS1):c.2167+9T>C rs1572822329
NM_005633.3(SOS1):c.225A>G (p.Gln75=) rs560037748
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.3(SOS1):c.2511-9dup rs727503436
NM_005633.3(SOS1):c.2541A>G (p.Glu847=) rs1572816424
NM_005633.3(SOS1):c.2674-16dup rs532594344
NM_005633.3(SOS1):c.2674-9del rs532594344
NM_005633.3(SOS1):c.273A>G (p.Gln91=) rs914110575
NM_005633.3(SOS1):c.2791+7_2791+10del rs760707217
NM_005633.3(SOS1):c.2868A>T (p.Ile956=) rs758834690
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.3093T>C (p.Tyr1031=) rs766864647
NM_005633.3(SOS1):c.3102C>A (p.Pro1034=) rs1572804715
NM_005633.3(SOS1):c.3132C>T (p.Asn1044=) rs544231079
NM_005633.3(SOS1):c.3195T>C (p.Tyr1065=) rs1280224224
NM_005633.3(SOS1):c.3330G>A (p.Ser1110=) rs146383828
NM_005633.3(SOS1):c.3330G>C (p.Ser1110=) rs146383828
NM_005633.3(SOS1):c.3357C>T (p.Thr1119=) rs373319212
NM_005633.3(SOS1):c.3387C>T (p.Gly1129=) rs772823827
NM_005633.3(SOS1):c.3504A>G (p.Pro1168=) rs748617507
NM_005633.3(SOS1):c.3777T>A (p.Pro1259=) rs1572796156
NM_005633.3(SOS1):c.3813G>A (p.Arg1271=) rs863224405
NM_005633.3(SOS1):c.3858C>T (p.Ser1286=) rs530210974
NM_005633.3(SOS1):c.396A>T (p.Ala132=) rs727505385
NM_005633.3(SOS1):c.39A>G (p.Glu13=) rs763337946
NM_005633.3(SOS1):c.511-9_511-6del rs986512473
NM_005633.3(SOS1):c.543A>G (p.Glu181=) rs201068374
NM_005633.3(SOS1):c.553A>G (p.Ile185Val) rs143962515
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
NM_005633.3(SOS1):c.783C>A (p.Gly261=) rs951992465
NM_005633.3(SOS1):c.891G>A (p.Ser297=) rs1572841459

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