ClinVar Miner

List of variants in gene SOS2 reported as likely benign for not provided

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Gene type:
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Total variants: 52
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HGVS dbSNP
NM_006939.4(SOS2):c.1005T>C (p.Tyr335=) rs753698896
NM_006939.4(SOS2):c.1198G>A (p.Asp400Asn) rs200368064
NM_006939.4(SOS2):c.1392C>T (p.Gly464=) rs188355135
NM_006939.4(SOS2):c.1443C>T (p.Tyr481=) rs755043578
NM_006939.4(SOS2):c.1593A>G (p.Glu531=) rs1414010933
NM_006939.4(SOS2):c.1767C>T (p.Asn589=) rs1427742827
NM_006939.4(SOS2):c.1785C>T (p.Gly595=) rs750732217
NM_006939.4(SOS2):c.1934+85_1934+88del rs201762253
NM_006939.4(SOS2):c.2014C>A (p.Leu672Ile) rs34139502
NM_006939.4(SOS2):c.2057+19_2057+20del rs111970905
NM_006939.4(SOS2):c.2137G>C (p.Glu713Gln) rs534384816
NM_006939.4(SOS2):c.2268T>G (p.Pro756=) rs1555369534
NM_006939.4(SOS2):c.2317G>C (p.Asp773His) rs114711076
NM_006939.4(SOS2):c.2328A>G (p.Thr776=) rs116162949
NM_006939.4(SOS2):c.2586T>C (p.Asp862=) rs1594969928
NM_006939.4(SOS2):c.2643A>G (p.Val881=) rs1329137002
NM_006939.4(SOS2):c.2646C>T (p.Tyr882=) rs761205651
NM_006939.4(SOS2):c.2668-86C>G rs74049160
NM_006939.4(SOS2):c.2740C>T (p.Leu914=) rs1363925093
NM_006939.4(SOS2):c.2786-4C>T rs1368282600
NM_006939.4(SOS2):c.2786-6T>C rs552609367
NM_006939.4(SOS2):c.294A>G (p.Lys98=) rs149713664
NM_006939.4(SOS2):c.2958+197G>T rs145761373
NM_006939.4(SOS2):c.2958+263G>A rs143771743
NM_006939.4(SOS2):c.2958+296G>A rs148973408
NM_006939.4(SOS2):c.2959-4C>G rs377396948
NM_006939.4(SOS2):c.3075+131A>G rs58543605
NM_006939.4(SOS2):c.3075+278del rs200433609
NM_006939.4(SOS2):c.3076-25C>T rs74049156
NM_006939.4(SOS2):c.3076-264G>A rs147840816
NM_006939.4(SOS2):c.3279A>C (p.Pro1093=) rs780697283
NM_006939.4(SOS2):c.3338-141G>C rs190371489
NM_006939.4(SOS2):c.3338-200T>C rs74744180
NM_006939.4(SOS2):c.346-194G>C rs74542284
NM_006939.4(SOS2):c.3555A>G (p.Val1185=) rs1594951532
NM_006939.4(SOS2):c.357G>A (p.Gly119=) rs749639774
NM_006939.4(SOS2):c.3606T>C (p.Ser1202=) rs539432390
NM_006939.4(SOS2):c.3729C>T (p.His1243=) rs761917783
NM_006939.4(SOS2):c.3762G>A (p.Thr1254=) rs769536087
NM_006939.4(SOS2):c.3774G>A (p.Ser1258=) rs747521589
NM_006939.4(SOS2):c.3945G>A (p.Ser1315=) rs143427064
NM_006939.4(SOS2):c.3981T>C (p.Asn1327=) rs527576404
NM_006939.4(SOS2):c.511-81G>A rs60775477
NM_006939.4(SOS2):c.540C>T (p.Asp180=) rs189555369
NM_006939.4(SOS2):c.600T>C (p.Tyr200=) rs766470992
NM_006939.4(SOS2):c.627A>G (p.Glu209=) rs771839900
NM_006939.4(SOS2):c.714+95G>A rs144846115
NM_006939.4(SOS2):c.804T>C (p.Thr268=) rs750437794
NM_006939.4(SOS2):c.858+40A>G rs148013479
NM_006939.4(SOS2):c.859-66C>G rs7146333
NM_006939.4(SOS2):c.88-142C>A rs148637943
NM_006939.4(SOS2):c.969+181G>T rs55847805

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