ClinVar Miner

List of variants in gene SOS1 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 106
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HGVS dbSNP gnomAD frequency
NM_005633.4(SOS1):c.2792-48T>C rs540132304 0.00865
NM_005633.4(SOS1):c.2997T>C (p.Asn999=) rs145364368 0.00352
NM_005633.4(SOS1):c.2673+14T>C rs183998234 0.00304
NM_005633.4(SOS1):c.213+16T>C rs150536159 0.00128
NM_005633.4(SOS1):c.2238T>C (p.Asn746=) rs75877625 0.00084
NM_005633.4(SOS1):c.749T>C (p.Val250Ala) rs139290271 0.00054
NM_005633.4(SOS1):c.2371C>A (p.Leu791Ile) rs142004123 0.00053
NM_005633.4(SOS1):c.2760G>A (p.Arg920=) rs149092581 0.00051
NM_005633.4(SOS1):c.345+12_345+13dup rs397517167 0.00050
NM_005633.4(SOS1):c.1203-13T>A rs145166996 0.00049
NM_005633.4(SOS1):c.698A>G (p.Asn233Ser) rs144934321 0.00026
NM_005633.4(SOS1):c.1770G>A (p.Glu590=) rs553331572 0.00022
NM_005633.4(SOS1):c.1705C>G (p.Leu569Val) rs200786705 0.00019
NM_005633.4(SOS1):c.3286T>A (p.Ser1096Thr) rs376722127 0.00017
NM_005633.4(SOS1):c.109A>G (p.Thr37Ala) rs150565592 0.00016
NM_005633.4(SOS1):c.2966G>A (p.Arg989Lys) rs202043599 0.00016
NM_005633.4(SOS1):c.3709C>G (p.Pro1237Ala) rs371408734 0.00016
NM_005633.4(SOS1):c.1962G>A (p.Glu654=) rs144382701 0.00014
NM_005633.4(SOS1):c.1668A>C (p.Val556=) rs376314461 0.00013
NM_005633.4(SOS1):c.1953A>G (p.Pro651=) rs141507912 0.00013
NM_005633.4(SOS1):c.3072C>T (p.Leu1024=) rs558386297 0.00013
NM_005633.4(SOS1):c.3330G>C (p.Ser1110=) rs146383828 0.00013
NM_005633.4(SOS1):c.3600C>G (p.Asp1200Glu) rs141594736 0.00013
NM_005633.4(SOS1):c.3946C>G (p.His1316Asp) rs371024396 0.00013
NM_005633.4(SOS1):c.3357C>T (p.Thr1119=) rs373319212 0.00011
NM_005633.4(SOS1):c.2165G>A (p.Arg722Lys) rs142666652 0.00010
NM_005633.4(SOS1):c.553A>G (p.Ile185Val) rs143962515 0.00010
NM_005633.4(SOS1):c.1829T>C (p.Ile610Thr) rs776146535 0.00007
NM_005633.4(SOS1):c.1854C>T (p.Tyr618=) rs727505181 0.00007
NM_005633.4(SOS1):c.3269C>T (p.Pro1090Leu) rs730881034 0.00007
NM_005633.4(SOS1):c.2168-50A>C rs778705378 0.00006
NM_005633.4(SOS1):c.2225T>C (p.Ile742Thr) rs767494615 0.00006
NM_005633.4(SOS1):c.1490G>A (p.Arg497Gln) rs371314838 0.00004
NM_005633.4(SOS1):c.1621T>C (p.Leu541=) rs371286473 0.00004
NM_005633.4(SOS1):c.1842G>A (p.Thr614=) rs143750479 0.00004
NM_005633.4(SOS1):c.3859A>G (p.Ile1287Val) rs760917490 0.00004
NM_005633.4(SOS1):c.162A>G (p.Gln54=) rs763520126 0.00003
NM_005633.4(SOS1):c.3802G>A (p.Gly1268Ser) rs730881051 0.00003
NM_005633.4(SOS1):c.3867G>A (p.Gly1289=) rs767844484 0.00003
NM_005633.4(SOS1):c.88-7T>A rs1416502603 0.00003
NM_005633.4(SOS1):c.1008A>G (p.Gln336=) rs1320092319 0.00002
NM_005633.4(SOS1):c.1251A>C (p.Leu417=) rs144027132 0.00002
NM_005633.4(SOS1):c.396A>T (p.Ala132=) rs727505385 0.00002
NM_005633.4(SOS1):c.899G>A (p.Arg300Gln) rs754374236 0.00002
NM_005633.4(SOS1):c.1047C>T (p.His349=) rs1043516636 0.00001
NM_005633.4(SOS1):c.1203-41C>T rs568590951 0.00001
NM_005633.4(SOS1):c.1278G>A (p.Gln426=) rs1352756240 0.00001
NM_005633.4(SOS1):c.1458A>G (p.Ala486=) rs772746896 0.00001
NM_005633.4(SOS1):c.1848T>C (p.His616=) rs1344852617 0.00001
NM_005633.4(SOS1):c.2604T>C (p.Phe868=) rs756520305 0.00001
NM_005633.4(SOS1):c.2728G>C (p.Asp910His) rs369277679 0.00001
NM_005633.4(SOS1):c.2739G>A (p.Lys913=) rs997339872 0.00001
NM_005633.4(SOS1):c.2838G>A (p.Glu946=) rs397517162 0.00001
NM_005633.4(SOS1):c.2868A>C (p.Ile956=) rs758834690 0.00001
NM_005633.4(SOS1):c.2999G>A (p.Ser1000Asn) rs891035934 0.00001
NM_005633.4(SOS1):c.3060C>T (p.Asn1020=) rs142431345 0.00001
NM_005633.4(SOS1):c.3093T>C (p.Tyr1031=) rs766864647 0.00001
NM_005633.4(SOS1):c.3114T>G (p.Pro1038=) rs777755307 0.00001
NM_005633.4(SOS1):c.3303T>C (p.Val1101=) rs397517165 0.00001
NM_005633.4(SOS1):c.3438A>G (p.Glu1146=) rs1226908698 0.00001
NM_005633.4(SOS1):c.350T>G (p.Val117Gly) rs201085754 0.00001
NM_005633.4(SOS1):c.3732T>C (p.His1244=) rs1391583247 0.00001
NM_005633.4(SOS1):c.3801C>T (p.His1267=) rs747676700 0.00001
NM_005633.4(SOS1):c.3832T>C (p.Leu1278=) rs750354913 0.00001
NM_005633.4(SOS1):c.429G>A (p.Lys143=) rs773264070 0.00001
NM_005633.4(SOS1):c.552T>C (p.Asn184=) rs727503438 0.00001
NM_005633.4(SOS1):c.675T>G (p.Val225=) rs371482290 0.00001
NM_005633.3(SOS1):c.2511-9dup rs727503436
NM_005633.4(SOS1):c.*12C>T rs1057522437
NM_005633.4(SOS1):c.*1606del rs34248802
NM_005633.4(SOS1):c.*2244_*2245dup rs3832123
NM_005633.4(SOS1):c.*8T>C rs1057521160
NM_005633.4(SOS1):c.1203-17C>G rs1553356202
NM_005633.4(SOS1):c.1293T>C (p.Gly431=)
NM_005633.4(SOS1):c.1434A>T (p.Pro478=) rs368495902
NM_005633.4(SOS1):c.1491A>G (p.Arg497=) rs1432437086
NM_005633.4(SOS1):c.1707G>A (p.Leu569=) rs1479407572
NM_005633.4(SOS1):c.1859-5_1859-3del rs1171459346
NM_005633.4(SOS1):c.1987A>G (p.Ile663Val) rs730881024
NM_005633.4(SOS1):c.2061G>A (p.Leu687=) rs727504752
NM_005633.4(SOS1):c.2063+44T>C rs111576630
NM_005633.4(SOS1):c.2064-20A>T rs756707478
NM_005633.4(SOS1):c.2127T>C (p.Tyr709=) rs1340535048
NM_005633.4(SOS1):c.214-18A>T
NM_005633.4(SOS1):c.2674-22C>G rs61601281
NM_005633.4(SOS1):c.2674-9T>C
NM_005633.4(SOS1):c.2775A>T (p.Pro925=) rs397517160
NM_005633.4(SOS1):c.2811C>T (p.Ile937=) rs1668929693
NM_005633.4(SOS1):c.3136A>C (p.Arg1046=) rs1668859268
NM_005633.4(SOS1):c.3195T>C (p.Tyr1065=) rs1280224224
NM_005633.4(SOS1):c.3321C>T (p.Ser1107=)
NM_005633.4(SOS1):c.3369A>G (p.Gln1123=) rs727503435
NM_005633.4(SOS1):c.3600C>T (p.Asp1200=) rs141594736
NM_005633.4(SOS1):c.360T>C (p.Tyr120=)
NM_005633.4(SOS1):c.3620C>G (p.Pro1207Arg) rs730881025
NM_005633.4(SOS1):c.3658G>A (p.Val1220Met) rs776814547
NM_005633.4(SOS1):c.3709C>A (p.Pro1237Thr) rs371408734
NM_005633.4(SOS1):c.375G>A (p.Gln125=) rs1400246247
NM_005633.4(SOS1):c.3876T>C (p.Val1292=) rs1423591930
NM_005633.4(SOS1):c.3948C>T (p.His1316=) rs1399242305
NM_005633.4(SOS1):c.396A>G (p.Ala132=) rs727505385
NM_005633.4(SOS1):c.483T>C (p.Asp161=) rs1553362598
NM_005633.4(SOS1):c.588A>T (p.Ser196=) rs727504826
NM_005633.4(SOS1):c.597A>G (p.Gln199=) rs397517175
NM_005633.4(SOS1):c.706T>C (p.Leu236=) rs1418372765
NM_005633.4(SOS1):c.976-5dup rs771586560

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