ClinVar Miner

List of variants in gene SOS1 reported by Integrated Genetics/Laboratory Corporation of America

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP
NM_005633.3(SOS1):c.*4C>T rs188849286
NM_005633.3(SOS1):c.1008A>G (p.Gln336=) rs1320092319
NM_005633.3(SOS1):c.1018C>T (p.Pro340Ser) rs190222208
NM_005633.3(SOS1):c.1047C>T (p.His349=) rs1043516636
NM_005633.3(SOS1):c.1203-20T>C rs112906251
NM_005633.3(SOS1):c.1269C>G (p.Asn423Lys) rs138459502
NM_005633.3(SOS1):c.1278G>A (p.Gln426=) rs1352756240
NM_005633.3(SOS1):c.1300G>A (p.Gly434Arg) rs397517148
NM_005633.3(SOS1):c.1310T>C (p.Ile437Thr) rs397517150
NM_005633.3(SOS1):c.1352C>G (p.Thr451Arg) rs730880218
NM_005633.3(SOS1):c.1370A>G (p.His457Arg) rs1060503524
NM_005633.3(SOS1):c.141T>C (p.Tyr47=) rs201649682
NM_005633.3(SOS1):c.1454A>G (p.Asn485Ser) rs140671910
NM_005633.3(SOS1):c.1490G>A (p.Arg497Gln) rs371314838
NM_005633.3(SOS1):c.1627T>C (p.Ser543Pro) rs981234810
NM_005633.3(SOS1):c.162A>G (p.Gln54=) rs763520126
NM_005633.3(SOS1):c.1646C>A (p.Thr549Lys) rs730881046
NM_005633.3(SOS1):c.1654A>G (p.Arg552Gly) rs137852814
NM_005633.3(SOS1):c.1655G>A (p.Arg552Lys) rs397517154
NM_005633.3(SOS1):c.1656G>T (p.Arg552Ser) rs267607079
NM_005633.3(SOS1):c.1668A>C (p.Val556=) rs376314461
NM_005633.3(SOS1):c.1719T>C (p.Asp573=) rs746674452
NM_005633.3(SOS1):c.1720G>A (p.Val574Ile) rs727504641
NM_005633.3(SOS1):c.1770G>A (p.Glu590=) rs553331572
NM_005633.3(SOS1):c.1820T>C (p.Ile607Thr) rs758699499
NM_005633.3(SOS1):c.1829T>C (p.Ile610Thr) rs776146535
NM_005633.3(SOS1):c.1854C>T (p.Tyr618=) rs727505181
NM_005633.3(SOS1):c.1867T>G (p.Phe623Val) rs727505093
NM_005633.3(SOS1):c.1931T>C (p.Ile644Thr) rs769891933
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.2127T>C (p.Tyr709=) rs1340535048
NM_005633.3(SOS1):c.213+9A>G rs553097014
NM_005633.3(SOS1):c.2165G>A (p.Arg722Lys) rs142666652
NM_005633.3(SOS1):c.2167+16del rs79984786
NM_005633.3(SOS1):c.2188G>T (p.Val730Phe) rs1558469016
NM_005633.3(SOS1):c.2197A>T (p.Ile733Phe) rs574088829
NM_005633.3(SOS1):c.2312T>C (p.Ile771Thr) rs557328600
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.3(SOS1):c.2489A>G (p.Asn830Ser) rs397517158
NM_005633.3(SOS1):c.2511-9T>A rs769427441
NM_005633.3(SOS1):c.2536G>A (p.Glu846Lys) rs397517159
NM_005633.3(SOS1):c.2606A>G (p.Asn869Ser) rs730881030
NM_005633.3(SOS1):c.2673+14T>C rs183998234
NM_005633.3(SOS1):c.2728G>C (p.Asp910His) rs369277679
NM_005633.3(SOS1):c.2788T>A (p.Phe930Ile) rs1558465734
NM_005633.3(SOS1):c.2791+7_2791+10del rs760707217
NM_005633.3(SOS1):c.2945G>A (p.Arg982Gln) rs1553351453
NM_005633.3(SOS1):c.2964+17A>G rs201906525
NM_005633.3(SOS1):c.2966G>A (p.Arg989Lys) rs202043599
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.3269C>T (p.Pro1090Leu) rs730881034
NM_005633.3(SOS1):c.3286T>A (p.Ser1096Thr) rs376722127
NM_005633.3(SOS1):c.3322G>C (p.Asp1108His) rs199856844
NM_005633.3(SOS1):c.3347-1G>A rs141565234
NM_005633.3(SOS1):c.3357C>T (p.Thr1119=) rs373319212
NM_005633.3(SOS1):c.3391+3T>C rs761579423
NM_005633.3(SOS1):c.3391+3_3391+6del rs756201866
NM_005633.3(SOS1):c.3391+7A>G rs201982464
NM_005633.3(SOS1):c.3412A>G (p.Ile1138Val) rs56248239
NM_005633.3(SOS1):c.3418T>A (p.Leu1140Ile) rs375550588
NM_005633.3(SOS1):c.345+12_345+13dup rs397517167
NM_005633.3(SOS1):c.345+15C>T rs75937422
NM_005633.3(SOS1):c.3510+9A>G rs1229357367
NM_005633.3(SOS1):c.3524A>C (p.His1175Pro) rs730881035
NM_005633.3(SOS1):c.3601C>T (p.Arg1201Trp) rs752395541
NM_005633.3(SOS1):c.3658G>T (p.Val1220Leu) rs776814547
NM_005633.3(SOS1):c.3709C>G (p.Pro1237Ala) rs371408734
NM_005633.3(SOS1):c.3724A>G (p.Ser1242Gly) rs1293079271
NM_005633.3(SOS1):c.3729C>G (p.Asp1243Glu) rs730881026
NM_005633.3(SOS1):c.376G>A (p.Val126Ile) rs755770649
NM_005633.3(SOS1):c.3832T>C (p.Leu1278=) rs750354913
NM_005633.3(SOS1):c.3857C>G (p.Ser1286Cys) rs374341202
NM_005633.3(SOS1):c.3857C>T (p.Ser1286Phe) rs374341202
NM_005633.3(SOS1):c.483T>C (p.Asp161=) rs1553362598
NM_005633.3(SOS1):c.508A>G (p.Lys170Glu) rs397517172
NM_005633.3(SOS1):c.510+10T>A rs1553362584
NM_005633.3(SOS1):c.510+9C>G rs553448375
NM_005633.3(SOS1):c.553A>G (p.Ile185Val) rs143962515
NM_005633.3(SOS1):c.638G>A (p.Arg213Gln) rs374761537
NM_005633.3(SOS1):c.688T>G (p.Phe230Val) rs397517177
NM_005633.3(SOS1):c.698A>G (p.Asn233Ser) rs144934321
NM_005633.3(SOS1):c.706T>C (p.Leu236=) rs1418372765
NM_005633.3(SOS1):c.720T>C (p.Asn240=) rs779699814
NM_005633.3(SOS1):c.749T>C (p.Val250Ala) rs139290271
NM_005633.3(SOS1):c.755T>C (p.Ile252Thr) rs142094234
NM_005633.3(SOS1):c.806T>C (p.Met269Thr) rs137852813
NM_005633.4(SOS1):c.1202+3G>A
NM_005633.4(SOS1):c.1251_1347dup (p.Leu450delinsSerAsnGlnGluAspGluArgAspSerGluGluTyrTer)
NM_005633.4(SOS1):c.1271_1345dup (p.Thr449_Leu450insLysIleGlnLysAsnIleAspGlyTrpGluGlyLysAspIleGlyGlnCysCysAsnGluPheIleMetGluGly)
NM_005633.4(SOS1):c.1940+18A>T
NM_005633.4(SOS1):c.2180A>G (p.Lys727Arg)
NM_005633.4(SOS1):c.2265_2355dup (p.Arg786delinsGluPheThrSerHisSerTer)
NM_005633.4(SOS1):c.2864_2944dup (p.Leu955_Leu981dup)
NM_005633.4(SOS1):c.2990T>C (p.Met997Thr)
NM_005633.4(SOS1):c.3136A>C (p.Arg1046=)
NM_005633.4(SOS1):c.3415A>G (p.Ser1139Gly)
NM_005633.4(SOS1):c.511-5T>C
NM_005633.4(SOS1):c.670A>G (p.Lys224Glu)

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