ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 113
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HGVS dbSNP
NM_005633.3(SOS1):c.*4C>T rs188849286
NM_005633.3(SOS1):c.1047C>T (p.His349=) rs1043516636
NM_005633.3(SOS1):c.104A>G (p.His35Arg) rs886041928
NM_005633.3(SOS1):c.1066C>T (p.Leu356Phe) rs1558480495
NM_005633.3(SOS1):c.1098T>A (p.Asp366Glu) rs730881040
NM_005633.3(SOS1):c.1230G>A (p.Gln410=) rs141390073
NM_005633.3(SOS1):c.1270G>A (p.Glu424Lys) rs730881041
NM_005633.3(SOS1):c.1271A>G (p.Glu424Gly) rs730881042
NM_005633.3(SOS1):c.127G>C (p.Asp43His) rs730881052
NM_005633.3(SOS1):c.1352C>G (p.Thr451Arg) rs730880218
NM_005633.3(SOS1):c.1374G>C (p.Glu458Asp) rs886042040
NM_005633.3(SOS1):c.143T>C (p.Val48Ala) rs373898570
NM_005633.3(SOS1):c.1442C>T (p.Pro481Leu) rs730880383
NM_005633.3(SOS1):c.1452C>A (p.Ser484Arg) rs730880384
NM_005633.3(SOS1):c.1490G>A (p.Arg497Gln) rs371314838
NM_005633.3(SOS1):c.1528T>C (p.Tyr510His) rs201404055
NM_005633.3(SOS1):c.1532A>G (p.Lys511Arg)
NM_005633.3(SOS1):c.1558G>T (p.Asp520Tyr)
NM_005633.3(SOS1):c.1559A>T (p.Asp520Val)
NM_005633.3(SOS1):c.1574T>C (p.Ile525Thr) rs146722878
NM_005633.3(SOS1):c.1626A>G (p.Ile542Met) rs746798986
NM_005633.3(SOS1):c.1627T>C (p.Ser543Pro) rs981234810
NM_005633.3(SOS1):c.1645A>G (p.Thr549Ala) rs1558474335
NM_005633.3(SOS1):c.1666G>A (p.Val556Ile)
NM_005633.3(SOS1):c.1668A>C (p.Val556=) rs376314461
NM_005633.3(SOS1):c.1720G>A (p.Val574Ile) rs727504641
NM_005633.3(SOS1):c.1760T>C (p.Ile587Thr) rs1553356018
NM_005633.3(SOS1):c.1802T>C (p.Ile601Thr) rs1558474155
NM_005633.3(SOS1):c.1820T>C (p.Ile607Thr) rs758699499
NM_005633.3(SOS1):c.1977T>A (p.Asp659Glu) rs1362181978
NM_005633.3(SOS1):c.199G>A (p.Ala67Thr) rs730881053
NM_005633.3(SOS1):c.2105A>G (p.Tyr702Cys) rs757094189
NM_005633.3(SOS1):c.2113G>A (p.Glu705Lys) rs730880385
NM_005633.3(SOS1):c.213+9A>G rs553097014
NM_005633.3(SOS1):c.2138G>A (p.Arg713Gln) rs483352826
NM_005633.3(SOS1):c.220G>A (p.Val74Ile) rs1292587800
NM_005633.3(SOS1):c.2227G>C (p.Ala743Pro) rs759584440
NM_005633.3(SOS1):c.2237A>G (p.Asn746Ser)
NM_005633.3(SOS1):c.2253T>G (p.Asn751Lys) rs1553354376
NM_005633.3(SOS1):c.2279C>T (p.Thr760Ile) rs730881027
NM_005633.3(SOS1):c.233T>G (p.Phe78Cys) rs201352584
NM_005633.3(SOS1):c.2345T>G (p.Ile782Arg)
NM_005633.3(SOS1):c.2391-8_2391-6del rs1558468009
NM_005633.3(SOS1):c.244A>G (p.Ile82Val) rs397517157
NM_005633.3(SOS1):c.2489A>G (p.Asn830Ser) rs397517158
NM_005633.3(SOS1):c.2490C>G (p.Asn830Lys) rs730881029
NM_005633.3(SOS1):c.2511-9dup rs727503436
NM_005633.3(SOS1):c.25G>A (p.Glu9Lys) rs1347187972
NM_005633.3(SOS1):c.2606A>G (p.Asn869Ser) rs730881030
NM_005633.3(SOS1):c.2616del (p.Glu873fs) rs1553353462
NM_005633.3(SOS1):c.2681C>G (p.Pro894Arg) rs1367714753
NM_005633.3(SOS1):c.2728G>C (p.Asp910His) rs369277679
NM_005633.3(SOS1):c.2836G>C (p.Glu946Gln) rs1558460847
NM_005633.3(SOS1):c.2945G>A (p.Arg982Gln) rs1553351453
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.3077G>A (p.Arg1026Lys) rs730881032
NM_005633.3(SOS1):c.3081T>A (p.Phe1027Leu) rs1553351362
NM_005633.3(SOS1):c.3148A>G (p.Met1050Val) rs886041814
NM_005633.3(SOS1):c.3197G>C (p.Ser1066Thr) rs1428068201
NM_005633.3(SOS1):c.3198T>G (p.Ser1066Arg) rs886041475
NM_005633.3(SOS1):c.3236C>T (p.Ala1079Val) rs730881033
NM_005633.3(SOS1):c.3242A>G (p.Asn1081Ser)
NM_005633.3(SOS1):c.3257C>T (p.Pro1086Leu) rs730881028
NM_005633.3(SOS1):c.3269dup (p.Pro1091fs) rs1057518017
NM_005633.3(SOS1):c.3282T>G (p.Gly1094=) rs145357714
NM_005633.3(SOS1):c.3290G>C (p.Ser1097Thr) rs727505379
NM_005633.3(SOS1):c.3322G>A (p.Asp1108Asn) rs199856844
NM_005633.3(SOS1):c.3322G>C (p.Asp1108His) rs199856844
NM_005633.3(SOS1):c.3329C>G (p.Ser1110Trp) rs572955351
NM_005633.3(SOS1):c.3347-1G>A rs141565234
NM_005633.3(SOS1):c.3387C>T (p.Gly1129=) rs772823827
NM_005633.3(SOS1):c.3391+7A>G rs201982464
NM_005633.3(SOS1):c.3412A>G (p.Ile1138Val) rs56248239
NM_005633.3(SOS1):c.3524A>C (p.His1175Pro) rs730881035
NM_005633.3(SOS1):c.3531C>A (p.Asp1177Glu) rs730881049
NM_005633.3(SOS1):c.3532A>G (p.Ser1178Gly) rs773306505
NM_005633.3(SOS1):c.3600C>G (p.Asp1200Glu) rs141594736
NM_005633.3(SOS1):c.3649C>T (p.Arg1217Ter) rs914233131
NM_005633.3(SOS1):c.3658G>T (p.Val1220Leu) rs776814547
NM_005633.3(SOS1):c.3697C>A (p.Leu1233Ile) rs777373438
NM_005633.3(SOS1):c.3721A>G (p.Lys1241Glu) rs367693130
NM_005633.3(SOS1):c.3724A>G (p.Ser1242Gly) rs1293079271
NM_005633.3(SOS1):c.3769A>G (p.Thr1257Ala) rs553805862
NM_005633.3(SOS1):c.3821C>G (p.Pro1274Arg) rs886041565
NM_005633.3(SOS1):c.3826C>T (p.Pro1276Ser) rs1064796575
NM_005633.3(SOS1):c.3857C>G (p.Ser1286Cys) rs374341202
NM_005633.3(SOS1):c.3896_3898del (p.Ser1299_Gln1300delinsTer) rs730881055
NM_005633.3(SOS1):c.3946C>G (p.His1316Asp) rs371024396
NM_005633.3(SOS1):c.3956T>G (p.Met1319Arg) rs730881036
NM_005633.3(SOS1):c.3960C>G (p.His1320Gln) rs1553349464
NM_005633.3(SOS1):c.39A>G (p.Glu13=) rs763337946
NM_005633.3(SOS1):c.483T>C (p.Asp161=) rs1553362598
NM_005633.3(SOS1):c.487A>G (p.Lys163Glu) rs886042206
NM_005633.3(SOS1):c.494C>G (p.Ala165Gly) rs1558492346
NM_005633.3(SOS1):c.510+10T>A rs1553362584
NM_005633.3(SOS1):c.544G>A (p.Asp182Asn) rs1553362279
NM_005633.3(SOS1):c.553A>G (p.Ile185Val) rs143962515
NM_005633.3(SOS1):c.571G>A (p.Glu191Lys) rs886041241
NM_005633.3(SOS1):c.638G>A (p.Arg213Gln) rs374761537
NM_005633.3(SOS1):c.642A>T (p.Gln214His) rs886041696
NM_005633.3(SOS1):c.669A>G (p.Ile223Met) rs1553362230
NM_005633.3(SOS1):c.698A>G (p.Asn233Ser) rs144934321
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.757C>T (p.His253Tyr) rs886041934
NM_005633.3(SOS1):c.788T>C (p.Ile263Thr) rs1310500908
NM_005633.3(SOS1):c.804_806del (p.Met269del)
NM_005633.3(SOS1):c.847T>C (p.Phe283Leu) rs1222945881
NM_005633.3(SOS1):c.890C>T (p.Ser297Leu) rs779162761
NM_005633.3(SOS1):c.938G>A (p.Ser313Asn)
NM_005633.3(SOS1):c.961G>A (p.Ala321Thr) rs1558480612

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