ClinVar Miner

List of variants in gene SOS2 reported as uncertain significance

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Gene type:
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Total variants: 152
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HGVS dbSNP
NC_000014.9:g.(?_50188487)_(50204419_?)dup
NM_006939.4(SOS2):c.1042T>G (p.Cys348Gly)
NM_006939.4(SOS2):c.1146A>G (p.Gln382=) rs1178247373
NM_006939.4(SOS2):c.1175A>G (p.Tyr392Cys) rs1085307558
NM_006939.4(SOS2):c.1181C>T (p.Pro394Leu)
NM_006939.4(SOS2):c.1189C>G (p.Arg397Gly)
NM_006939.4(SOS2):c.1264G>A (p.Glu422Lys)
NM_006939.4(SOS2):c.1266A>C (p.Glu422Asp)
NM_006939.4(SOS2):c.1273A>G (p.Lys425Glu) rs372203654
NM_006939.4(SOS2):c.1320T>A (p.Asn440Lys)
NM_006939.4(SOS2):c.1331T>C (p.Met444Thr)
NM_006939.4(SOS2):c.133_136del (p.Leu45fs)
NM_006939.4(SOS2):c.13C>G (p.Pro5Ala)
NM_006939.4(SOS2):c.1417C>T (p.His473Tyr)
NM_006939.4(SOS2):c.1427C>T (p.Thr476Ile)
NM_006939.4(SOS2):c.1429C>T (p.Arg477Trp) rs1555370121
NM_006939.4(SOS2):c.142A>G (p.Ile48Val) rs763552267
NM_006939.4(SOS2):c.1550A>G (p.Lys517Arg) rs367970301
NM_006939.4(SOS2):c.1567A>G (p.Ile523Val)
NM_006939.4(SOS2):c.1634G>A (p.Arg545His)
NM_006939.4(SOS2):c.1859A>G (p.Asn620Ser)
NM_006939.4(SOS2):c.185C>T (p.Ala62Val)
NM_006939.4(SOS2):c.1861T>G (p.Phe621Val) rs1555370029
NM_006939.4(SOS2):c.1868G>A (p.Arg623His) rs138459515
NM_006939.4(SOS2):c.1895T>G (p.Phe632Cys)
NM_006939.4(SOS2):c.189G>C (p.Gln63His)
NM_006939.4(SOS2):c.1900A>G (p.Lys634Glu)
NM_006939.4(SOS2):c.1976T>C (p.Leu659Ser)
NM_006939.4(SOS2):c.2068G>A (p.Val690Ile)
NM_006939.4(SOS2):c.2113G>T (p.Asp705Tyr) rs1057518079
NM_006939.4(SOS2):c.2128G>C (p.Glu710Gln) rs768829374
NM_006939.4(SOS2):c.213+7A>C
NM_006939.4(SOS2):c.2161+10A>G rs201629454
NM_006939.4(SOS2):c.2162-27_2231dup
NM_006939.4(SOS2):c.2168C>T (p.Ala723Val) rs1566827698
NM_006939.4(SOS2):c.220G>A (p.Val74Ile)
NM_006939.4(SOS2):c.2221G>A (p.Ala741Thr) rs1594973893
NM_006939.4(SOS2):c.2228C>G (p.Ala743Gly) rs752871832
NM_006939.4(SOS2):c.2234_2278dup (p.Gly745_Ile759dup)
NM_006939.4(SOS2):c.2246A>G (p.Asn749Ser) rs761689009
NM_006939.4(SOS2):c.2261G>A (p.Ser754Asn) rs181275468
NM_006939.4(SOS2):c.2264C>T (p.Pro755Leu)
NM_006939.4(SOS2):c.2290A>G (p.Ser764Gly)
NM_006939.4(SOS2):c.2299G>A (p.Gly767Arg) rs886041953
NM_006939.4(SOS2):c.2304G>T (p.Gln768His) rs778281839
NM_006939.4(SOS2):c.230C>G (p.Thr77Ser)
NM_006939.4(SOS2):c.2312_2313insTGTCCT (p.Phe772_Asp773insValLeu)
NM_006939.4(SOS2):c.2315T>G (p.Phe772Cys)
NM_006939.4(SOS2):c.2318A>C (p.Asp773Ala)
NM_006939.4(SOS2):c.2347G>T (p.Ala783Ser)
NM_006939.4(SOS2):c.2366T>C (p.Leu789Ser) rs142863840
NM_006939.4(SOS2):c.2384+5A>G rs376903120
NM_006939.4(SOS2):c.2385-3T>C
NM_006939.4(SOS2):c.2396C>T (p.Pro799Leu) rs773672997
NM_006939.4(SOS2):c.2443A>G (p.Asn815Asp) rs886041958
NM_006939.4(SOS2):c.257C>T (p.Ala86Val) rs146272145
NM_006939.4(SOS2):c.2600A>G (p.Asn867Ser) rs561495878
NM_006939.4(SOS2):c.2602G>A (p.Gly868Ser) rs751419448
NM_006939.4(SOS2):c.2606T>C (p.Val869Ala) rs750095346
NM_006939.4(SOS2):c.2621G>A (p.Ser874Asn) rs1057518082
NM_006939.4(SOS2):c.2657A>G (p.His886Arg)
NM_006939.4(SOS2):c.2668-5T>C
NM_006939.4(SOS2):c.2707G>A (p.Val903Met)
NM_006939.4(SOS2):c.2758A>G (p.Ile920Val) rs755783805
NM_006939.4(SOS2):c.2843A>G (p.Lys948Arg)
NM_006939.4(SOS2):c.2849G>A (p.Gly950Glu)
NM_006939.4(SOS2):c.290G>A (p.Arg97Gln) rs777574895
NM_006939.4(SOS2):c.2957G>A (p.Arg986Lys) rs772746106
NM_006939.4(SOS2):c.2958+17C>T
NM_006939.4(SOS2):c.2959-20T>G
NM_006939.4(SOS2):c.2969A>G (p.Glu990Gly) rs761320331
NM_006939.4(SOS2):c.2978A>T (p.Asn993Ile) rs776000121
NM_006939.4(SOS2):c.2980C>G (p.Pro994Ala)
NM_006939.4(SOS2):c.2981C>G (p.Pro994Arg)
NM_006939.4(SOS2):c.2983A>G (p.Met995Val) rs933544183
NM_006939.4(SOS2):c.2986G>A (p.Gly996Arg)
NM_006939.4(SOS2):c.3026A>G (p.Asn1009Ser)
NM_006939.4(SOS2):c.3076-3C>T
NM_006939.4(SOS2):c.3076C>T (p.Pro1026Ser) rs201874067
NM_006939.4(SOS2):c.3114A>G (p.Ile1038Met)
NM_006939.4(SOS2):c.3157C>T (p.Arg1053Ter)
NM_006939.4(SOS2):c.3172C>T (p.Pro1058Ser)
NM_006939.4(SOS2):c.3190T>C (p.Cys1064Arg)
NM_006939.4(SOS2):c.322G>A (p.Asp108Asn) rs1566477432
NM_006939.4(SOS2):c.3235A>G (p.Thr1079Ala) rs61755576
NM_006939.4(SOS2):c.3266C>A (p.Pro1089Gln) rs1409054252
NM_006939.4(SOS2):c.3275C>T (p.Pro1092Leu) rs1442962879
NM_006939.4(SOS2):c.3277C>T (p.Pro1093Ser)
NM_006939.4(SOS2):c.3302G>A (p.Ser1101Asn)
NM_006939.4(SOS2):c.3337+4A>G
NM_006939.4(SOS2):c.3338-4A>G rs777684425
NM_006939.4(SOS2):c.3338-6C>G
NM_006939.4(SOS2):c.3356C>T (p.Ala1119Val)
NM_006939.4(SOS2):c.3379+1G>C rs1566818889
NM_006939.4(SOS2):c.3380-3_3380-2del
NM_006939.4(SOS2):c.3383C>G (p.Ser1128Cys) rs1566815476
NM_006939.4(SOS2):c.338C>T (p.Ser113Leu)
NM_006939.4(SOS2):c.3403A>G (p.Ser1135Gly) rs375478974
NM_006939.4(SOS2):c.3407T>C (p.Leu1136Ser)
NM_006939.4(SOS2):c.3443_3454del (p.Pro1148_Pro1151del)
NM_006939.4(SOS2):c.346-3C>T
NM_006939.4(SOS2):c.3520G>A (p.Ala1174Thr)
NM_006939.4(SOS2):c.3553G>T (p.Val1185Leu)
NM_006939.4(SOS2):c.3560C>T (p.Pro1187Leu) rs1594951526
NM_006939.4(SOS2):c.3571G>C (p.Val1191Leu)
NM_006939.4(SOS2):c.3584C>T (p.Ala1195Val) rs753151750
NM_006939.4(SOS2):c.3644C>G (p.Thr1215Ser)
NM_006939.4(SOS2):c.364G>A (p.Val122Met)
NM_006939.4(SOS2):c.3741C>G (p.Asp1247Glu)
NM_006939.4(SOS2):c.3755_3757del (p.Ile1252del) rs775506222
NM_006939.4(SOS2):c.3758G>C (p.Ser1253Thr)
NM_006939.4(SOS2):c.3761C>G (p.Thr1254Arg) rs772587016
NM_006939.4(SOS2):c.3781A>C (p.Thr1261Pro) rs1555367637
NM_006939.4(SOS2):c.3788C>G (p.Pro1263Arg)
NM_006939.4(SOS2):c.3818G>A (p.Arg1273Gln)
NM_006939.4(SOS2):c.3845A>G (p.Asn1282Ser)
NM_006939.4(SOS2):c.3868C>G (p.Pro1290Ala)
NM_006939.4(SOS2):c.3902A>G (p.His1301Arg)
NM_006939.4(SOS2):c.390T>G (p.Ile130Met)
NM_006939.4(SOS2):c.3944C>T (p.Ser1315Leu)
NM_006939.4(SOS2):c.3957G>T (p.Leu1319Phe)
NM_006939.4(SOS2):c.3968C>T (p.Pro1323Leu) rs886041929
NM_006939.4(SOS2):c.3997T>C (p.Ter1333Arg)
NM_006939.4(SOS2):c.432G>A (p.Leu144=) rs1051166055
NM_006939.4(SOS2):c.458G>A (p.Arg153Gln)
NM_006939.4(SOS2):c.496A>G (p.Met166Val) rs1555322175
NM_006939.4(SOS2):c.502G>A (p.Ala168Thr)
NM_006939.4(SOS2):c.516G>C (p.Leu172Phe)
NM_006939.4(SOS2):c.523A>C (p.Met175Leu)
NM_006939.4(SOS2):c.530A>G (p.Asp177Gly)
NM_006939.4(SOS2):c.533A>C (p.Gln178Pro) rs1273376869
NM_006939.4(SOS2):c.536A>G (p.Asp179Gly) rs770997822
NM_006939.4(SOS2):c.542T>C (p.Ile181Thr)
NM_006939.4(SOS2):c.572C>A (p.Pro191His)
NM_006939.4(SOS2):c.572C>T (p.Pro191Leu) rs72681869
NM_006939.4(SOS2):c.574A>G (p.Ser192Gly)
NM_006939.4(SOS2):c.622G>T (p.Ala208Ser) rs61755579
NM_006939.4(SOS2):c.624_673dup (p.Arg225delinsGlnLysLysAspSerIleTyrGlyAsnTer)
NM_006939.4(SOS2):c.643C>T (p.Arg215Trp)
NM_006939.4(SOS2):c.674G>A (p.Arg225Gln) rs780580623
NM_006939.4(SOS2):c.714T>G (p.Ser238=) rs750665891
NM_006939.4(SOS2):c.721G>A (p.Glu241Lys) rs148747022
NM_006939.4(SOS2):c.769_858+8dup
NM_006939.4(SOS2):c.780G>T (p.Leu260Phe) rs1348457314
NM_006939.4(SOS2):c.811A>G (p.Ser271Gly)
NM_006939.4(SOS2):c.839G>C (p.Cys280Ser) rs530007285
NM_006939.4(SOS2):c.842T>C (p.Phe281Ser) rs1555371627
NM_006939.4(SOS2):c.940G>A (p.Ala314Thr)
NM_006939.4(SOS2):c.970-14T>A
NM_006939.4(SOS2):c.970-24_1037dup
NM_006939.4(SOS2):c.973A>T (p.Ile325Phe) rs1594993511
NM_006939.4(SOS2):c.985_1064dup (p.Lys356fs)

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