ClinVar Miner

List of variants in gene SOS2 reported as likely benign

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Gene type:
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Total variants: 138
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HGVS dbSNP
NM_006939.4(SOS2):c.1005T>C (p.Tyr335=) rs753698896
NM_006939.4(SOS2):c.1059G>A (p.Glu353=)
NM_006939.4(SOS2):c.1071A>G (p.Gln357=) rs111961549
NM_006939.4(SOS2):c.1176T>C (p.Tyr392=) rs1555370242
NM_006939.4(SOS2):c.1197-8T>G
NM_006939.4(SOS2):c.1198G>A (p.Asp400Asn) rs200368064
NM_006939.4(SOS2):c.1281C>T (p.Ile427=)
NM_006939.4(SOS2):c.1339C>A (p.Pro447Thr)
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.1446T>C (p.Ser482=)
NM_006939.4(SOS2):c.147A>G (p.Glu49=) rs1030329651
NM_006939.4(SOS2):c.1515T>C (p.Thr505=)
NM_006939.4(SOS2):c.1521G>T (p.Glu507Asp) rs141604342
NM_006939.4(SOS2):c.1593A>G (p.Glu531=) rs1414010933
NM_006939.4(SOS2):c.1669T>C (p.Leu557=)
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.1815G>T (p.Val605=)
NM_006939.4(SOS2):c.1839T>C (p.Tyr613=)
NM_006939.4(SOS2):c.1853-10G>A
NM_006939.4(SOS2):c.1884A>C (p.Thr628=)
NM_006939.4(SOS2):c.1889G>A (p.Arg630His) rs754778456
NM_006939.4(SOS2):c.1934+85_1934+88del rs201762253
NM_006939.4(SOS2):c.195G>A (p.Arg65=) rs1803661
NM_006939.4(SOS2):c.1989A>G (p.Lys663=)
NM_006939.4(SOS2):c.2007T>C (p.Ser669=) rs577622341
NM_006939.4(SOS2):c.2010A>G (p.Ala670=)
NM_006939.4(SOS2):c.2014C>A (p.Leu672Ile) rs34139502
NM_006939.4(SOS2):c.2057+19T>A rs544924513
NM_006939.4(SOS2):c.2057+19_2057+20del rs111970905
NM_006939.4(SOS2):c.2058-10A>G
NM_006939.4(SOS2):c.2115C>T (p.Asp705=)
NM_006939.4(SOS2):c.2120A>G (p.Glu707Gly) rs369462490
NM_006939.4(SOS2):c.213+10A>G
NM_006939.4(SOS2):c.2137G>C (p.Glu713Gln) rs534384816
NM_006939.4(SOS2):c.2154T>C (p.Ser718=) rs568511771
NM_006939.4(SOS2):c.2162-10C>T rs375702667
NM_006939.4(SOS2):c.2190A>G (p.Ser730=)
NM_006939.4(SOS2):c.2217G>A (p.Lys739=) rs186110427
NM_006939.4(SOS2):c.2220A>C (p.Gln740His)
NM_006939.4(SOS2):c.2261G>A (p.Ser754Asn) rs181275468
NM_006939.4(SOS2):c.2268T>G (p.Pro756=) rs1555369534
NM_006939.4(SOS2):c.2271A>G (p.Pro757=)
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.2604C>T (p.Gly868=) rs765945171
NM_006939.4(SOS2):c.2640A>G (p.Ser880=) rs146730136
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.2700C>T (p.Asp900=)
NM_006939.4(SOS2):c.2712A>G (p.Glu904=) rs143332839
NM_006939.4(SOS2):c.2740C>T (p.Leu914=) rs1363925093
NM_006939.4(SOS2):c.2786-17_2786-16insTC
NM_006939.4(SOS2):c.2786-18_2786-17dup
NM_006939.4(SOS2):c.2786-4C>T rs1368282600
NM_006939.4(SOS2):c.2786-5dup
NM_006939.4(SOS2):c.2786-6T>A rs552609367
NM_006939.4(SOS2):c.2786-6T>C rs552609367
NM_006939.4(SOS2):c.2854G>A (p.Asp952Asn) rs200387871
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.3051A>C (p.Arg1017=)
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.3079A>C (p.Arg1027=)
NM_006939.4(SOS2):c.3088A>G (p.Thr1030Ala) rs550680554
NM_006939.4(SOS2):c.3138C>T (p.Gly1046=)
NM_006939.4(SOS2):c.3235A>G (p.Thr1079Ala) rs61755576
NM_006939.4(SOS2):c.3250A>G (p.Thr1084Ala) rs150752193
NM_006939.4(SOS2):c.3279A>C (p.Pro1093=) rs780697283
NM_006939.4(SOS2):c.3289T>C (p.Ser1097Pro)
NM_006939.4(SOS2):c.3338-141G>C rs190371489
NM_006939.4(SOS2):c.3338-200T>C rs74744180
NM_006939.4(SOS2):c.3338-8del
NM_006939.4(SOS2):c.3360A>C (p.Pro1120=)
NM_006939.4(SOS2):c.339G>A (p.Ser113=)
NM_006939.4(SOS2):c.340T>C (p.Leu114=)
NM_006939.4(SOS2):c.346-194G>C rs74542284
NM_006939.4(SOS2):c.3495T>C (p.Asn1165=)
NM_006939.4(SOS2):c.3503C>A (p.Ser1168Tyr) rs143166880
NM_006939.4(SOS2):c.3540T>G (p.Pro1180=)
NM_006939.4(SOS2):c.3555A>G (p.Val1185=) rs1594951532
NM_006939.4(SOS2):c.3573T>G (p.Val1191=)
NM_006939.4(SOS2):c.357G>A (p.Gly119=) rs749639774
NM_006939.4(SOS2):c.3588T>C (p.Phe1196=)
NM_006939.4(SOS2):c.3606T>C (p.Ser1202=) rs539432390
NM_006939.4(SOS2):c.360C>T (p.Tyr120=) rs762044455
NM_006939.4(SOS2):c.3614C>T (p.Pro1205Leu) rs113660113
NM_006939.4(SOS2):c.3615G>A (p.Pro1205=)
NM_006939.4(SOS2):c.3729C>T (p.His1243=) rs761917783
NM_006939.4(SOS2):c.3744G>T (p.Trp1248Cys) rs138133010
NM_006939.4(SOS2):c.3755_3757del (p.Ile1252del) rs775506222
NM_006939.4(SOS2):c.3762G>A (p.Thr1254=) rs769536087
NM_006939.4(SOS2):c.3769A>G (p.Asn1257Asp) rs150393358
NM_006939.4(SOS2):c.3774G>A (p.Ser1258=) rs747521589
NM_006939.4(SOS2):c.3824A>G (p.Tyr1275Cys) rs371619971
NM_006939.4(SOS2):c.3825T>C (p.Tyr1275=)
NM_006939.4(SOS2):c.3830T>C (p.Leu1277Pro) rs146802994
NM_006939.4(SOS2):c.384A>G (p.Leu128=) rs772264111
NM_006939.4(SOS2):c.3945G>A (p.Ser1315=) rs143427064
NM_006939.4(SOS2):c.3952C>T (p.Pro1318Ser) rs140995728
NM_006939.4(SOS2):c.3954A>G (p.Pro1318=)
NM_006939.4(SOS2):c.396T>C (p.Ala132=) rs774402309
NM_006939.4(SOS2):c.3981T>C (p.Asn1327=) rs527576404
NM_006939.4(SOS2):c.399A>C (p.Val133=) rs144584870
NM_006939.4(SOS2):c.399A>G (p.Val133=) rs144584870
NM_006939.4(SOS2):c.453T>C (p.Asn151=)
NM_006939.4(SOS2):c.511-81G>A rs60775477
NM_006939.4(SOS2):c.540C>T (p.Asp180=) rs189555369
NM_006939.4(SOS2):c.549G>C (p.Leu183Phe) rs137961578
NM_006939.4(SOS2):c.572C>G (p.Pro191Arg) rs72681869
NM_006939.4(SOS2):c.584G>C (p.Gly195Ala)
NM_006939.4(SOS2):c.599A>G (p.Tyr200Cys) rs148595463
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.702G>A (p.Leu234=) rs200208472
NM_006939.4(SOS2):c.709C>A (p.Pro237Thr)
NM_006939.4(SOS2):c.714+95G>A rs144846115
NM_006939.4(SOS2):c.753T>C (p.His251=)
NM_006939.4(SOS2):c.804T>C (p.Thr268=) rs750437794
NM_006939.4(SOS2):c.813C>T (p.Ser271=)
NM_006939.4(SOS2):c.837C>T (p.Ser279=) rs542617984
NM_006939.4(SOS2):c.858+40A>G rs148013479
NM_006939.4(SOS2):c.859-10A>T rs761341096
NM_006939.4(SOS2):c.859-66C>G rs7146333
NM_006939.4(SOS2):c.88-142C>A rs148637943
NM_006939.4(SOS2):c.894G>A (p.Gln298=)
NM_006939.4(SOS2):c.958C>T (p.Leu320=)
NM_006939.4(SOS2):c.969+181G>T rs55847805
NM_006939.4(SOS2):c.969+20T>G rs559272877

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