ClinVar Miner

List of variants in gene SOS1 reported as uncertain significance for not specified

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Gene type:
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Total variants: 126
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HGVS dbSNP gnomAD frequency
NM_005633.4(SOS1):c.749T>C (p.Val250Ala) rs139290271 0.00054
NM_005633.4(SOS1):c.1705C>G (p.Leu569Val) rs200786705 0.00019
NM_005633.4(SOS1):c.*4C>T rs188849286 0.00018
NM_005633.4(SOS1):c.3347-1G>A rs141565234 0.00017
NM_005633.4(SOS1):c.3706C>A (p.Pro1236Thr) rs727504636 0.00016
NM_005633.4(SOS1):c.3418T>A (p.Leu1140Ile) rs375550588 0.00010
NM_005633.4(SOS1):c.553A>G (p.Ile185Val) rs143962515 0.00010
NM_005633.4(SOS1):c.214-17T>C rs369722808 0.00009
NM_005633.4(SOS1):c.244A>G (p.Ile82Val) rs397517157 0.00009
NM_005633.4(SOS1):c.3322G>A (p.Asp1108Asn) rs199856844 0.00009
NM_005633.4(SOS1):c.3269C>T (p.Pro1090Leu) rs730881034 0.00007
NM_005633.4(SOS1):c.3729C>G (p.Asp1243Glu) rs730881026 0.00007
NM_005633.4(SOS1):c.929G>A (p.Arg310His) rs143481916 0.00006
NM_005633.4(SOS1):c.2312T>C (p.Ile771Thr) rs557328600 0.00005
NM_005633.4(SOS1):c.587C>T (p.Ser196Leu) rs199898869 0.00005
NM_005633.4(SOS1):c.841A>G (p.Ser281Gly) rs397517178 0.00005
NM_005633.4(SOS1):c.1490G>A (p.Arg497Gln) rs371314838 0.00004
NM_005633.4(SOS1):c.1720G>A (p.Val574Ile) rs727504641 0.00004
NM_005633.4(SOS1):c.2587C>A (p.Gln863Lys) rs141501083 0.00004
NM_005633.4(SOS1):c.3392G>A (p.Arg1131Lys) rs768113420 0.00004
NM_005633.4(SOS1):c.3857C>T (p.Ser1286Phe) rs374341202 0.00004
NM_005633.4(SOS1):c.3703C>T (p.Pro1235Ser) rs397517168 0.00003
NM_005633.4(SOS1):c.1010A>G (p.Tyr337Cys) rs724160007 0.00002
NM_005633.4(SOS1):c.2062C>A (p.Arg688=) rs186246534 0.00002
NM_005633.4(SOS1):c.3412A>G (p.Ile1138Val) rs56248239 0.00002
NM_005633.4(SOS1):c.3836C>T (p.Thr1279Ile) rs758258471 0.00002
NM_005633.4(SOS1):c.1202+3G>A rs904487658 0.00001
NM_005633.4(SOS1):c.1385T>A (p.Phe462Tyr) rs730881043 0.00001
NM_005633.4(SOS1):c.1412G>C (p.Cys471Ser) rs397517151 0.00001
NM_005633.4(SOS1):c.1564A>C (p.Asn522His) rs761094509 0.00001
NM_005633.4(SOS1):c.1627T>C (p.Ser543Pro) rs981234810 0.00001
NM_005633.4(SOS1):c.1931T>C (p.Ile644Thr) rs769891933 0.00001
NM_005633.4(SOS1):c.2064-15G>T rs746484679 0.00001
NM_005633.4(SOS1):c.2391-17T>C rs551161418 0.00001
NM_005633.4(SOS1):c.2489A>G (p.Asn830Ser) rs397517158 0.00001
NM_005633.4(SOS1):c.2511-9T>A rs769427441 0.00001
NM_005633.4(SOS1):c.281T>C (p.Ile94Thr) rs397517161 0.00001
NM_005633.4(SOS1):c.2990T>C (p.Met997Thr) rs1321926273 0.00001
NM_005633.4(SOS1):c.2998A>T (p.Ser1000Cys) rs730881031 0.00001
NM_005633.4(SOS1):c.2999G>A (p.Ser1000Asn) rs891035934 0.00001
NM_005633.4(SOS1):c.3257C>T (p.Pro1086Leu) rs730881028 0.00001
NM_005633.4(SOS1):c.350T>G (p.Val117Gly) rs201085754 0.00001
NM_005633.4(SOS1):c.3510+9A>G rs1229357367 0.00001
NM_005633.4(SOS1):c.3662G>C (p.Arg1221Thr) rs768987761 0.00001
NM_005633.4(SOS1):c.3721A>G (p.Lys1241Glu) rs367693130 0.00001
NM_005633.4(SOS1):c.3734G>T (p.Gly1245Val) rs397517169 0.00001
NM_005633.4(SOS1):c.3763C>A (p.Pro1255Thr) rs972166211 0.00001
NM_005633.4(SOS1):c.376G>A (p.Val126Ile) rs755770649 0.00001
NM_005633.4(SOS1):c.3905T>C (p.Ile1302Thr) rs750296853 0.00001
NM_005633.4(SOS1):c.511-5T>C rs1558491271 0.00001
NM_005633.4(SOS1):c.571G>A (p.Glu191Lys) rs886041241 0.00001
NM_005633.4(SOS1):c.688T>G (p.Phe230Val) rs397517177 0.00001
NM_005633.4(SOS1):c.754A>C (p.Ile252Leu) rs1158811958 0.00001
NM_005633.4(SOS1):c.847T>C (p.Phe283Leu) rs1222945881 0.00001
NM_005633.4(SOS1):c.88-14C>G rs727504900 0.00001
NM_005633.4(SOS1):c.985G>A (p.Glu329Lys) rs756679265 0.00001
NM_005633.4(SOS1):c.1063G>A (p.Glu355Lys) rs1670303340
NM_005633.4(SOS1):c.1199T>G (p.Leu400Arg)
NM_005633.4(SOS1):c.1251_1347dup (p.Leu450delinsSerAsnGlnGluAspGluArgAspSerGluGluTyrTer) rs1669848601
NM_005633.4(SOS1):c.1269C>G (p.Asn423Lys) rs138459502
NM_005633.4(SOS1):c.1271_1345dup (p.Gly448_Thr449insLysIleGlnLysAsnIleAspGlyTrpGluGlyLysAspIleGlyGlnCysCysAsnGluPheIleMetGluGly) rs1669848769
NM_005633.4(SOS1):c.1288G>A (p.Asp430Asn)
NM_005633.4(SOS1):c.1370A>G (p.His457Arg) rs1060503524
NM_005633.4(SOS1):c.1391T>C (p.Phe464Ser)
NM_005633.4(SOS1):c.1412G>A (p.Cys471Tyr) rs397517151
NM_005633.4(SOS1):c.1412G>T (p.Cys471Phe)
NM_005633.4(SOS1):c.1429C>A (p.Gln477Lys) rs397517152
NM_005633.4(SOS1):c.1433C>T (p.Pro478Leu) rs1553356111
NM_005633.4(SOS1):c.1454A>G (p.Asn485Ser) rs140671910
NM_005633.4(SOS1):c.1459G>A (p.Glu487Lys) rs1057517897
NM_005633.4(SOS1):c.1499A>C (p.Gln500Pro) rs2124537167
NM_005633.4(SOS1):c.1600A>G (p.Lys534Glu) rs1669840891
NM_005633.4(SOS1):c.1646C>A (p.Thr549Lys) rs730881046
NM_005633.4(SOS1):c.1690G>A (p.Glu564Lys) rs1386900583
NM_005633.4(SOS1):c.1727G>T (p.Arg576Ile) rs1553356023
NM_005633.4(SOS1):c.1759A>G (p.Ile587Val)
NM_005633.4(SOS1):c.1867T>G (p.Phe623Val) rs727505093
NM_005633.4(SOS1):c.1880T>G (p.Phe627Cys) rs1057518197
NM_005633.4(SOS1):c.1940+18A>T rs1669577494
NM_005633.4(SOS1):c.1954G>C (p.Glu652Gln) rs1408868952
NM_005633.4(SOS1):c.2045T>C (p.Ile682Thr)
NM_005633.4(SOS1):c.2051C>T (p.Pro684Leu) rs397517155
NM_005633.4(SOS1):c.2057A>G (p.Gln686Arg)
NM_005633.4(SOS1):c.214-12C>T rs2124610999
NM_005633.4(SOS1):c.2168G>T (p.Gly723Val)
NM_005633.4(SOS1):c.2180A>G (p.Lys727Arg) rs1669496540
NM_005633.4(SOS1):c.2188G>T (p.Val730Phe) rs1558469016
NM_005633.4(SOS1):c.2200A>C (p.Thr734Pro) rs727503437
NM_005633.4(SOS1):c.2227G>A (p.Ala743Thr)
NM_005633.4(SOS1):c.2265_2355dup (p.Arg786delinsGluPheThrSerHisSerTer) rs1669491885
NM_005633.4(SOS1):c.2405C>T (p.Ser802Leu)
NM_005633.4(SOS1):c.2489A>T (p.Asn830Ile) rs397517158
NM_005633.4(SOS1):c.2490C>A (p.Asn830Lys) rs730881029
NM_005633.4(SOS1):c.2708A>C (p.Glu903Ala)
NM_005633.4(SOS1):c.2762C>G (p.Ser921Cys) rs1553353332
NM_005633.4(SOS1):c.2788T>A (p.Phe930Ile) rs1558465734
NM_005633.4(SOS1):c.2791+19A>C
NM_005633.4(SOS1):c.2791+7_2791+10del rs760707217
NM_005633.4(SOS1):c.2792-4C>G
NM_005633.4(SOS1):c.2864_2944dup (p.Leu955_Leu981dup) rs1668926020
NM_005633.4(SOS1):c.2918A>T (p.Gln973Leu) rs727505016
NM_005633.4(SOS1):c.3256C>T (p.Pro1086Ser) rs1057517892
NM_005633.4(SOS1):c.3290G>A (p.Ser1097Asn) rs727505379
NM_005633.4(SOS1):c.3319T>G (p.Ser1107Ala)
NM_005633.4(SOS1):c.3391+3_3391+6del rs756201866
NM_005633.4(SOS1):c.3406T>A (p.Ser1136Thr) rs2124458840
NM_005633.4(SOS1):c.3415A>G (p.Ser1139Gly) rs1668593642
NM_005633.4(SOS1):c.348G>A (p.Glu116=) rs1671231096
NM_005633.4(SOS1):c.3568A>G (p.Lys1190Glu) rs1553349579
NM_005633.4(SOS1):c.3580C>T (p.Pro1194Ser)
NM_005633.4(SOS1):c.3600C>A (p.Asp1200Glu) rs141594736
NM_005633.4(SOS1):c.3601C>T (p.Arg1201Trp) rs752395541
NM_005633.4(SOS1):c.3696T>G (p.His1232Gln)
NM_005633.4(SOS1):c.3709C>A (p.Pro1237Thr) rs371408734
NM_005633.4(SOS1):c.373C>A (p.Gln125Lys) rs397517170
NM_005633.4(SOS1):c.3952T>A (p.Ser1318Thr) rs397517171
NM_005633.4(SOS1):c.3971C>G (p.Pro1324Arg) rs727503434
NM_005633.4(SOS1):c.416C>G (p.Ala139Gly) rs1671229011
NM_005633.4(SOS1):c.440A>T (p.Asn147Ile)
NM_005633.4(SOS1):c.511-12_511-11del rs397517173
NM_005633.4(SOS1):c.512T>G (p.Val171Gly) rs397517174
NM_005633.4(SOS1):c.668T>C (p.Ile223Thr) rs397517176
NM_005633.4(SOS1):c.670A>G (p.Lys224Glu) rs889231089
NM_005633.4(SOS1):c.743G>A (p.Arg248His)
NM_005633.4(SOS1):c.788T>C (p.Ile263Thr) rs1310500908
NM_005633.4(SOS1):c.829C>A (p.Pro277Thr) rs1057517871

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