ClinVar Miner

List of variants in gene SOS1 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP
NM_005633.3(SOS1):c.*12C>T rs1057522437
NM_005633.3(SOS1):c.*1606delT rs34248802
NM_005633.3(SOS1):c.*2244_*2245dupTA rs3832123
NM_005633.3(SOS1):c.*8T>C rs1057521160
NM_005633.3(SOS1):c.-43C>T rs1016843875
NM_005633.3(SOS1):c.109A>G (p.Thr37Ala) rs150565592
NM_005633.3(SOS1):c.1202+5A>G rs1021449471
NM_005633.3(SOS1):c.1203-13T>A rs145166996
NM_005633.3(SOS1):c.1203-17C>G rs1553356202
NM_005633.3(SOS1):c.1203-41C>T rs568590951
NM_005633.3(SOS1):c.1434A>T (p.Pro478=) rs368495902
NM_005633.3(SOS1):c.1458A>G (p.Ala486=) rs772746896
NM_005633.3(SOS1):c.1491A>G (p.Arg497=) rs1432437086
NM_005633.3(SOS1):c.1621T>C (p.Leu541=) rs371286473
NM_005633.3(SOS1):c.162A>G (p.Gln54=) rs763520126
NM_005633.3(SOS1):c.1705C>G (p.Leu569Val) rs200786705
NM_005633.3(SOS1):c.1707G>A (p.Leu569=) rs1479407572
NM_005633.3(SOS1):c.1770G>A (p.Glu590=) rs553331572
NM_005633.3(SOS1):c.1842G>A (p.Thr614=) rs143750479
NM_005633.3(SOS1):c.1848T>C (p.His616=) rs1344852617
NM_005633.3(SOS1):c.1854C>T (p.Tyr618=) rs727505181
NM_005633.3(SOS1):c.1859-5_1859-3delCTT rs1171459346
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.1987A>G (p.Ile663Val) rs730881024
NM_005633.3(SOS1):c.2061G>A (p.Leu687=) rs727504752
NM_005633.3(SOS1):c.2063+44T>C rs111576630
NM_005633.3(SOS1):c.2064-20A>T rs756707478
NM_005633.3(SOS1):c.213+16T>C rs150536159
NM_005633.3(SOS1):c.2168-50A>C rs778705378
NM_005633.3(SOS1):c.21C>T (p.Pro7=) rs727504845
NM_005633.3(SOS1):c.2238T>C (p.Asn746=) rs75877625
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.3(SOS1):c.2511-9dup rs727503436
NM_005633.3(SOS1):c.2673+14T>C rs183998234
NM_005633.3(SOS1):c.2674-22C>G rs61601281
NM_005633.3(SOS1):c.2674-9dup rs532594344
NM_005633.3(SOS1):c.2739G>A (p.Lys913=) rs997339872
NM_005633.3(SOS1):c.2760G>A (p.Arg920=) rs149092581
NM_005633.3(SOS1):c.2775A>T (p.Pro925=) rs397517160
NM_005633.3(SOS1):c.2792-48T>C rs540132304
NM_005633.3(SOS1):c.2838G>A (p.Glu946=) rs397517162
NM_005633.3(SOS1):c.2868A>C (p.Ile956=) rs758834690
NM_005633.3(SOS1):c.2966G>A (p.Arg989Lys) rs202043599
NM_005633.3(SOS1):c.2997T>C (p.Asn999=) rs145364368
NM_005633.3(SOS1):c.2999G>A (p.Ser1000Asn) rs891035934
NM_005633.3(SOS1):c.3060C>T (p.Asn1020=) rs142431345
NM_005633.3(SOS1):c.3072C>T (p.Leu1024=) rs558386297
NM_005633.3(SOS1):c.3269C>T (p.Pro1090Leu) rs730881034
NM_005633.3(SOS1):c.3303T>C (p.Val1101=) rs397517165
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.3369A>G (p.Gln1123=) rs727503435
NM_005633.3(SOS1):c.345+12_345+13dupCT rs397517167
NM_005633.3(SOS1):c.350T>G (p.Val117Gly) rs201085754
NM_005633.3(SOS1):c.3511-14_3511-10delTTTTC rs760713912
NM_005633.3(SOS1):c.3600C>T (p.Asp1200=) rs141594736
NM_005633.3(SOS1):c.3620C>G (p.Pro1207Arg) rs730881025
NM_005633.3(SOS1):c.3729C>G (p.Asp1243Glu) rs730881026
NM_005633.3(SOS1):c.3801C>T (p.His1267=) rs747676700
NM_005633.3(SOS1):c.3802G>A (p.Gly1268Ser) rs730881051
NM_005633.3(SOS1):c.3859A>G (p.Ile1287Val) rs760917490
NM_005633.3(SOS1):c.3900A>G (p.Gln1300=) rs1343754754
NM_005633.3(SOS1):c.3948C>T (p.His1316=) rs1399242305
NM_005633.3(SOS1):c.396A>T (p.Ala132=) rs727505385
NM_005633.3(SOS1):c.552T>C (p.Asn184=) rs727503438
NM_005633.3(SOS1):c.553A>G (p.Ile185Val) rs143962515
NM_005633.3(SOS1):c.588A>T (p.Ser196=) rs727504826
NM_005633.3(SOS1):c.597A>G (p.Gln199=) rs397517175
NM_005633.3(SOS1):c.688T>G (p.Phe230Val) rs397517177
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.87+12G>T rs368569135
NM_005633.3(SOS1):c.87+9C>T rs397517179
NM_005633.3(SOS1):c.88-7T>A rs1416502603
NM_005633.3(SOS1):c.899G>A (p.Arg300Gln) rs754374236
NM_005633.3(SOS1):c.976-5dupT rs771586560

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