ClinVar Miner

List of variants in gene SOS2 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_006939.4(SOS2):c.88-11010G>C rs117294554 0.00855
NM_006939.4(SOS2):c.591A>G (p.Leu197=) rs113460230 0.00834
NM_006939.4(SOS2):c.3075+7C>T rs144391749 0.00743
NM_006939.4(SOS2):c.572C>G (p.Pro191Arg) rs72681869 0.00416
NM_006939.4(SOS2):c.1344G>A (p.Leu448=) rs35530861 0.00350
NM_006939.4(SOS2):c.858+9A>G rs201701595 0.00101
NM_006939.4(SOS2):c.549G>C (p.Leu183Phe) rs137961578 0.00083
NM_006939.4(SOS2):c.1071A>G (p.Gln357=) rs111961549 0.00044
NM_006939.4(SOS2):c.3744G>T (p.Trp1248Cys) rs138133010 0.00041
NM_006939.4(SOS2):c.3830T>C (p.Leu1277Pro) rs146802994 0.00037
NM_006939.4(SOS2):c.2854G>A (p.Asp952Asn) rs200387871 0.00033
NM_006939.4(SOS2):c.3952C>T (p.Pro1318Ser) rs140995728 0.00029
NM_006939.4(SOS2):c.2640A>G (p.Ser880=) rs146730136 0.00027
NM_006939.4(SOS2):c.294A>G (p.Lys98=) rs149713664 0.00025
NM_006939.4(SOS2):c.2712A>G (p.Glu904=) rs143332839 0.00020
NM_006939.4(SOS2):c.3769A>G (p.Asn1257Asp) rs150393358 0.00017
NM_006939.4(SOS2):c.195G>A (p.Arg65=) rs1803661 0.00013
NM_006939.4(SOS2):c.702G>A (p.Leu234=) rs200208472 0.00012
NM_006939.4(SOS2):c.1263T>C (p.Asn421=) rs369267864 0.00011
NM_006939.4(SOS2):c.3088A>G (p.Thr1030Ala) rs550680554 0.00010
NM_006939.4(SOS2):c.674G>A (p.Arg225Gln) rs780580623 0.00006
NM_006939.4(SOS2):c.837C>T (p.Ser279=) rs542617984 0.00005
NM_006939.4(SOS2):c.3076C>T (p.Pro1026Ser) rs201874067 0.00004
NM_006939.4(SOS2):c.3584C>T (p.Ala1195Val) rs753151750 0.00004
NM_006939.4(SOS2):c.1612G>A (p.Ala538Thr) rs765427688 0.00002
NM_006939.4(SOS2):c.2604C>T (p.Gly868=) rs765945171 0.00002
NM_006939.4(SOS2):c.3698A>C (p.Asn1233Thr) rs201756168 0.00002
NM_006939.4(SOS2):c.3774G>A (p.Ser1258=) rs747521589 0.00002
NM_006939.4(SOS2):c.1446T>C (p.Ser482=) rs1468565433 0.00001
NM_006939.4(SOS2):c.1965C>T (p.Asp655=) rs763672521 0.00001
NM_006939.4(SOS2):c.2324T>C (p.Met775Thr) rs745868017 0.00001
NM_006939.4(SOS2):c.2741T>A (p.Leu914Gln) rs376313150 0.00001
NM_006939.4(SOS2):c.1127C>G (p.Thr376Ser) rs869320687
NM_006939.4(SOS2):c.1610C>T (p.Ala537Val) rs2502989298
NM_006939.4(SOS2):c.1861T>G (p.Phe621Val) rs1555370029
NM_006939.4(SOS2):c.2057+20TA[6] rs374223259
NM_006939.4(SOS2):c.2057+40TA[6] rs111550293
NM_006939.4(SOS2):c.2217G>T (p.Lys739Asn) rs186110427
NM_006939.4(SOS2):c.2786-18_2786-17dup rs201957103
NM_006939.4(SOS2):c.2832T>C (p.Asp944=) rs2502878370
NM_006939.4(SOS2):c.3540TCC[4] (p.Pro1183dup) rs765097073
NM_006939.4(SOS2):c.3706C>T (p.Pro1236Ser) rs2502757277
NM_006939.4(SOS2):c.3805A>G (p.Arg1269Gly) rs2502755779
NM_006939.4(SOS2):c.3930del (p.Thr1309_Tyr1310insTer) rs2139463075
NM_006939.4(SOS2):c.3961A>C (p.Arg1321=)
NM_006939.4(SOS2):c.556C>G (p.Leu186Val) rs2139734457
NM_006939.4(SOS2):c.622G>A (p.Ala208Thr) rs61755579
NM_006939.4(SOS2):c.693T>C (p.Asp231=) rs2139733831
NM_006939.4(SOS2):c.859-4del rs776327707

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