ClinVar Miner

List of variants in gene SOS1 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 167
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HGVS dbSNP gnomAD frequency
NM_005633.4(SOS1):c.3347-1G>A rs141565234 0.00017
NM_005633.4(SOS1):c.3709C>G (p.Pro1237Ala) rs371408734 0.00016
NM_005633.4(SOS1):c.3769A>G (p.Thr1257Ala) rs553805862 0.00006
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.2571G>C (p.Glu857Asp) rs757460662 0.00004
NM_005633.4(SOS1):c.3392G>A (p.Arg1131Lys) rs768113420 0.00004
NM_005633.4(SOS1):c.3737A>G (p.Asn1246Ser) rs374110460 0.00004
NM_005633.4(SOS1):c.1558G>A (p.Asp520Asn) rs754115060 0.00003
NM_005633.4(SOS1):c.1988T>C (p.Ile663Thr) rs1048869073 0.00003
NM_005633.4(SOS1):c.3697C>A (p.Leu1233Ile) rs777373438 0.00003
NM_005633.4(SOS1):c.1010A>G (p.Tyr337Cys) rs724160007 0.00002
NM_005633.4(SOS1):c.169A>T (p.Asn57Tyr) rs765764610 0.00002
NM_005633.4(SOS1):c.2138G>A (p.Arg713Gln) rs483352826 0.00002
NM_005633.4(SOS1):c.3148A>G (p.Met1050Val) rs886041814 0.00002
NM_005633.4(SOS1):c.3412A>G (p.Ile1138Val) rs56248239 0.00002
NM_005633.4(SOS1):c.3821C>G (p.Pro1274Arg) rs886041565 0.00002
NM_005633.4(SOS1):c.755T>C (p.Ile252Thr) rs142094234 0.00002
NM_005633.4(SOS1):c.1271A>G (p.Glu424Gly) rs730881042 0.00001
NM_005633.4(SOS1):c.127G>C (p.Asp43His) rs730881052 0.00001
NM_005633.4(SOS1):c.1303A>G (p.Lys435Glu) rs138920742 0.00001
NM_005633.4(SOS1):c.1385T>A (p.Phe462Tyr) rs730881043 0.00001
NM_005633.4(SOS1):c.1574T>C (p.Ile525Thr) rs146722878 0.00001
NM_005633.4(SOS1):c.1626A>G (p.Ile542Met) rs746798986 0.00001
NM_005633.4(SOS1):c.1627T>C (p.Ser543Pro) rs981234810 0.00001
NM_005633.4(SOS1):c.1768G>A (p.Glu590Lys) rs730881047 0.00001
NM_005633.4(SOS1):c.1802T>C (p.Ile601Thr) rs1558474155 0.00001
NM_005633.4(SOS1):c.1983A>G (p.Ile661Met) rs747203627 0.00001
NM_005633.4(SOS1):c.199G>A (p.Ala67Thr) rs730881053 0.00001
NM_005633.4(SOS1):c.2105A>G (p.Tyr702Cys) rs757094189 0.00001
NM_005633.4(SOS1):c.2158A>G (p.Thr720Ala) rs367634525 0.00001
NM_005633.4(SOS1):c.2227G>C (p.Ala743Pro) rs759584440 0.00001
NM_005633.4(SOS1):c.2279C>T (p.Thr760Ile) rs730881027 0.00001
NM_005633.4(SOS1):c.2382T>A (p.Asp794Glu) rs1317203797 0.00001
NM_005633.4(SOS1):c.2489A>G (p.Asn830Ser) rs397517158 0.00001
NM_005633.4(SOS1):c.2606A>G (p.Asn869Ser) rs730881030 0.00001
NM_005633.4(SOS1):c.2684G>A (p.Ser895Asn) rs1164976822 0.00001
NM_005633.4(SOS1):c.2964+6T>C rs766305289 0.00001
NM_005633.4(SOS1):c.3197G>C (p.Ser1066Thr) rs1428068201 0.00001
NM_005633.4(SOS1):c.3257C>T (p.Pro1086Leu) rs730881028 0.00001
NM_005633.4(SOS1):c.3290G>C (p.Ser1097Thr) rs727505379 0.00001
NM_005633.4(SOS1):c.3413T>A (p.Ile1138Lys) rs1433351757 0.00001
NM_005633.4(SOS1):c.3524A>C (p.His1175Pro) rs730881035 0.00001
NM_005633.4(SOS1):c.3531C>A (p.Asp1177Glu) rs730881049 0.00001
NM_005633.4(SOS1):c.3707C>T (p.Pro1236Leu) rs533661246 0.00001
NM_005633.4(SOS1):c.3721A>G (p.Lys1241Glu) rs367693130 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.571G>A (p.Glu191Lys) rs886041241 0.00001
NM_005633.4(SOS1):c.688T>G (p.Phe230Val) rs397517177 0.00001
NM_005633.4(SOS1):c.847T>C (p.Phe283Leu) rs1222945881 0.00001
NM_005633.4(SOS1):c.1007A>T (p.Gln336Leu) rs765028553
NM_005633.4(SOS1):c.104A>G (p.His35Arg) rs886041928
NM_005633.4(SOS1):c.1051C>G (p.Leu351Val)
NM_005633.4(SOS1):c.1063G>A (p.Glu355Lys) rs1670303340
NM_005633.4(SOS1):c.1066C>T (p.Leu356Phe) rs1558480495
NM_005633.4(SOS1):c.107C>T (p.Pro36Leu) rs2148140667
NM_005633.4(SOS1):c.1096G>T (p.Asp366Tyr) rs1669882172
NM_005633.4(SOS1):c.1098T>A (p.Asp366Glu) rs730881040
NM_005633.4(SOS1):c.1214G>A (p.Cys405Tyr) rs1005855156
NM_005633.4(SOS1):c.1264A>G (p.Met422Val)
NM_005633.4(SOS1):c.1269C>G (p.Asn423Lys) rs138459502
NM_005633.4(SOS1):c.1270G>A (p.Glu424Lys) rs730881041
NM_005633.4(SOS1):c.1333A>G (p.Ile445Val) rs2124537533
NM_005633.4(SOS1):c.1352C>G (p.Thr451Arg) rs730880218
NM_005633.4(SOS1):c.135dup (p.Gln46fs)
NM_005633.4(SOS1):c.1374G>C (p.Glu458Asp) rs886042040
NM_005633.4(SOS1):c.1459G>A (p.Glu487Lys) rs1057517897
NM_005633.4(SOS1):c.1543G>A (p.Glu515Lys)
NM_005633.4(SOS1):c.1558G>T (p.Asp520Tyr) rs754115060
NM_005633.4(SOS1):c.1594G>A (p.Glu532Lys)
NM_005633.4(SOS1):c.1630_1633delinsAAAA (p.Leu544_Gln545delinsLysLys) rs2124536829
NM_005633.4(SOS1):c.1645A>G (p.Thr549Ala) rs1558474335
NM_005633.4(SOS1):c.1666G>A (p.Val556Ile) rs753909912
NM_005633.4(SOS1):c.1686G>T (p.Glu562Asp) rs199778219
NM_005633.4(SOS1):c.1690G>A (p.Glu564Lys) rs1386900583
NM_005633.4(SOS1):c.1691A>G (p.Glu564Gly)
NM_005633.4(SOS1):c.1706T>C (p.Leu569Pro) rs2124536533
NM_005633.4(SOS1):c.1750G>A (p.Glu584Lys)
NM_005633.4(SOS1):c.1760T>C (p.Ile587Thr) rs1553356018
NM_005633.4(SOS1):c.1770G>C (p.Glu590Asp) rs553331572
NM_005633.4(SOS1):c.1795C>A (p.Pro599Thr)
NM_005633.4(SOS1):c.1798A>C (p.Ile600Leu) rs373139450
NM_005633.4(SOS1):c.183A>C (p.Gln61His) rs1355644577
NM_005633.4(SOS1):c.1880T>G (p.Phe627Cys) rs1057518197
NM_005633.4(SOS1):c.1977T>A (p.Asp659Glu) rs1362181978
NM_005633.4(SOS1):c.2063G>A (p.Arg688Gln) rs2124518275
NM_005633.4(SOS1):c.2089_2097delinsTTAGAGCAA (p.Val697_His699delinsLeuGluGln) rs2124517603
NM_005633.4(SOS1):c.2167+5del rs2124517396
NM_005633.4(SOS1):c.220G>A (p.Val74Ile) rs1292587800
NM_005633.4(SOS1):c.2237A>G (p.Asn746Ser) rs975491573
NM_005633.4(SOS1):c.2253T>G (p.Asn751Lys) rs1553354376
NM_005633.4(SOS1):c.2356C>T (p.Arg786Ter) rs2124514851
NM_005633.4(SOS1):c.2391-13T>C rs761268670
NM_005633.4(SOS1):c.2391-8_2391-6del rs1558468009
NM_005633.4(SOS1):c.2447T>C (p.Ile816Thr)
NM_005633.4(SOS1):c.2489A>T (p.Asn830Ile) rs397517158
NM_005633.4(SOS1):c.2490C>G (p.Asn830Lys) rs730881029
NM_005633.4(SOS1):c.2491C>G (p.Leu831Val) rs2124511437
NM_005633.4(SOS1):c.2680C>T (p.Pro894Ser) rs2124501972
NM_005633.4(SOS1):c.2681C>G (p.Pro894Arg) rs1367714753
NM_005633.4(SOS1):c.2874T>G (p.Phe958Leu) rs2124479605
NM_005633.4(SOS1):c.289A>G (p.Arg97Gly)
NM_005633.4(SOS1):c.3002T>C (p.Met1001Thr) rs2124478911
NM_005633.4(SOS1):c.3077G>A (p.Arg1026Lys) rs730881032
NM_005633.4(SOS1):c.3081T>A (p.Phe1027Leu) rs1553351362
NM_005633.4(SOS1):c.3082-6C>A rs2124475838
NM_005633.4(SOS1):c.3116G>A (p.Gly1039Asp) rs2124475752
NM_005633.4(SOS1):c.3198T>G (p.Ser1066Arg) rs886041475
NM_005633.4(SOS1):c.3220G>C (p.Glu1074Gln)
NM_005633.4(SOS1):c.3236C>T (p.Ala1079Val) rs730881033
NM_005633.4(SOS1):c.3242A>G (p.Asn1081Ser) rs992722303
NM_005633.4(SOS1):c.3256C>G (p.Pro1086Ala) rs1057517892
NM_005633.4(SOS1):c.3269dup (p.Pro1091fs) rs1057518017
NM_005633.4(SOS1):c.3276_3295del (p.Ser1093fs)
NM_005633.4(SOS1):c.3290G>A (p.Ser1097Asn) rs727505379
NM_005633.4(SOS1):c.3314T>C (p.Phe1105Ser) rs2124475147
NM_005633.4(SOS1):c.3329C>G (p.Ser1110Trp) rs572955351
NM_005633.4(SOS1):c.3382C>T (p.His1128Tyr) rs762576997
NM_005633.4(SOS1):c.3391+3_3391+6del rs756201866
NM_005633.4(SOS1):c.3451C>T (p.Pro1151Ser) rs2124458641
NM_005633.4(SOS1):c.3472C>T (p.Arg1158Ter)
NM_005633.4(SOS1):c.3508A>C (p.Lys1170Gln) rs1668590878
NM_005633.4(SOS1):c.3532A>G (p.Ser1178Gly) rs773306505
NM_005633.4(SOS1):c.3533G>C (p.Ser1178Thr) rs1050237569
NM_005633.4(SOS1):c.3534T>A (p.Ser1178Arg) rs1572796568
NM_005633.4(SOS1):c.3649C>T (p.Arg1217Ter) rs914233131
NM_005633.4(SOS1):c.3656C>G (p.Pro1219Arg)
NM_005633.4(SOS1):c.369C>G (p.Asp123Glu) rs1444978665
NM_005633.4(SOS1):c.3703C>A (p.Pro1235Thr) rs397517168
NM_005633.4(SOS1):c.3722A>G (p.Lys1241Arg)
NM_005633.4(SOS1):c.3766T>G (p.Phe1256Val) rs2124454889
NM_005633.4(SOS1):c.3770C>T (p.Thr1257Ile) rs962478091
NM_005633.4(SOS1):c.3794CTC[1] (p.Pro1266del) rs1272230145
NM_005633.4(SOS1):c.3826C>T (p.Pro1276Ser) rs1064796575
NM_005633.4(SOS1):c.3832T>A (p.Leu1278Met)
NM_005633.4(SOS1):c.3869C>T (p.Pro1290Leu)
NM_005633.4(SOS1):c.3896_3898del (p.Ser1299_Gln1300delinsTer) rs730881055
NM_005633.4(SOS1):c.3952T>A (p.Ser1318Thr) rs397517171
NM_005633.4(SOS1):c.3956T>G (p.Met1319Arg) rs730881036
NM_005633.4(SOS1):c.3960C>G (p.His1320Gln) rs1553349464
NM_005633.4(SOS1):c.3974C>T (p.Pro1325Leu)
NM_005633.4(SOS1):c.3977T>C (p.Leu1326Pro) rs1371048349
NM_005633.4(SOS1):c.494C>G (p.Ala165Gly) rs1558492346
NM_005633.4(SOS1):c.508A>C (p.Lys170Gln)
NM_005633.4(SOS1):c.544G>A (p.Asp182Asn) rs1553362279
NM_005633.4(SOS1):c.642A>T (p.Gln214His) rs886041696
NM_005633.4(SOS1):c.651G>T (p.Arg217Ser)
NM_005633.4(SOS1):c.669A>G (p.Ile223Met) rs1553362230
NM_005633.4(SOS1):c.670A>G (p.Lys224Glu) rs889231089
NM_005633.4(SOS1):c.676T>A (p.Phe226Ile)
NM_005633.4(SOS1):c.754A>G (p.Ile252Val) rs1158811958
NM_005633.4(SOS1):c.757C>T (p.His253Tyr) rs886041934
NM_005633.4(SOS1):c.788T>C (p.Ile263Thr) rs1310500908
NM_005633.4(SOS1):c.800T>C (p.Val267Ala)
NM_005633.4(SOS1):c.800_811del (p.Val267_Thr270del)
NM_005633.4(SOS1):c.802G>C (p.Glu268Gln)
NM_005633.4(SOS1):c.821G>C (p.Ser274Thr)
NM_005633.4(SOS1):c.829C>A (p.Pro277Thr) rs1057517871
NM_005633.4(SOS1):c.835G>T (p.Val279Leu)
NM_005633.4(SOS1):c.844T>C (p.Cys282Arg) rs1671004485
NM_005633.4(SOS1):c.845G>T (p.Cys282Phe)
NM_005633.4(SOS1):c.898C>A (p.Arg300=)
NM_005633.4(SOS1):c.911G>T (p.Arg304Leu) rs886254041
NM_005633.4(SOS1):c.961G>A (p.Ala321Thr) rs1558480612
NM_005633.4(SOS1):c.967T>C (p.Tyr323His) rs1670309576

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