ClinVar Miner

List of variants in gene SOS2 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_006939.4(SOS2):c.674G>A (p.Arg225Gln) rs780580623 0.00006
NM_006939.4(SOS2):c.3076C>T (p.Pro1026Ser) rs201874067 0.00004
NM_006939.4(SOS2):c.1273A>G (p.Lys425Glu) rs372203654 0.00001
NM_006939.4(SOS2):c.142A>G (p.Ile48Val) rs763552267 0.00001
NM_006939.4(SOS2):c.2443A>G (p.Asn815Asp) rs886041958 0.00001
NM_006939.4(SOS2):c.2471G>A (p.Arg824His) rs1433825913 0.00001
NM_006939.4(SOS2):c.536A>G (p.Asp179Gly) rs770997822 0.00001
NM_006939.4(SOS2):c.997G>A (p.Val333Ile) rs778569253 0.00001
NM_006939.4(SOS2):c.1022T>C (p.Met341Thr)
NM_006939.4(SOS2):c.1094A>C (p.Gln365Pro) rs2139636244
NM_006939.4(SOS2):c.1130C>T (p.Ala377Val)
NM_006939.4(SOS2):c.1175A>G (p.Tyr392Cys) rs1085307558
NM_006939.4(SOS2):c.1196+6del
NM_006939.4(SOS2):c.1266A>C (p.Glu422Asp) rs755550719
NM_006939.4(SOS2):c.1295_1296delinsTT (p.Gly432Val)
NM_006939.4(SOS2):c.1375A>G (p.Ile459Val) rs886268693
NM_006939.4(SOS2):c.1477G>A (p.Val493Ile)
NM_006939.4(SOS2):c.1550A>G (p.Lys517Arg) rs367970301
NM_006939.4(SOS2):c.1771C>T (p.Gln591Ter) rs2139628062
NM_006939.4(SOS2):c.1849G>C (p.Ala617Pro)
NM_006939.4(SOS2):c.1855C>A (p.Pro619Thr)
NM_006939.4(SOS2):c.1930G>A (p.Glu644Lys)
NM_006939.4(SOS2):c.2113G>T (p.Asp705Tyr) rs1057518079
NM_006939.4(SOS2):c.214-8T>C rs1886471396
NM_006939.4(SOS2):c.2228C>G (p.Ala743Gly) rs752871832
NM_006939.4(SOS2):c.2299G>A (p.Gly767Arg) rs886041953
NM_006939.4(SOS2):c.2417T>C (p.Val806Ala)
NM_006939.4(SOS2):c.2525A>G (p.Asn842Ser) rs2139576928
NM_006939.4(SOS2):c.2621G>A (p.Ser874Asn) rs1057518082
NM_006939.4(SOS2):c.2953A>G (p.Met985Val)
NM_006939.4(SOS2):c.3043G>A (p.Glu1015Lys) rs2139528697
NM_006939.4(SOS2):c.3130C>T (p.Arg1044Ter) rs1178530624
NM_006939.4(SOS2):c.3187C>A (p.Pro1063Thr) rs2139512845
NM_006939.4(SOS2):c.322G>A (p.Asp108Asn) rs1566477432
NM_006939.4(SOS2):c.3302G>A (p.Ser1101Asn) rs1419463844
NM_006939.4(SOS2):c.3379+1G>C rs1566818889
NM_006939.4(SOS2):c.3410A>G (p.His1137Arg)
NM_006939.4(SOS2):c.3452C>G (p.Pro1151Arg)
NM_006939.4(SOS2):c.346G>A (p.Glu116Lys)
NM_006939.4(SOS2):c.3513T>G (p.Asp1171Glu)
NM_006939.4(SOS2):c.3530C>T (p.Pro1177Leu) rs1566814839
NM_006939.4(SOS2):c.3626G>A (p.Arg1209Lys)
NM_006939.4(SOS2):c.3719G>C (p.Gly1240Ala)
NM_006939.4(SOS2):c.3928T>C (p.Tyr1310His)
NM_006939.4(SOS2):c.3957G>T (p.Leu1319Phe) rs2139462748
NM_006939.4(SOS2):c.3968C>T (p.Pro1323Leu) rs886041929
NM_006939.4(SOS2):c.500G>A (p.Cys167Tyr) rs1283726128
NM_006939.4(SOS2):c.521A>G (p.Asp174Gly) rs2139734704
NM_006939.4(SOS2):c.572C>T (p.Pro191Leu) rs72681869
NM_006939.4(SOS2):c.584G>C (p.Gly195Ala)
NM_006939.4(SOS2):c.614C>T (p.Thr205Ile) rs763214818
NM_006939.4(SOS2):c.775G>A (p.Gly259Ser)
NM_006939.4(SOS2):c.842T>C (p.Phe281Ser) rs1555371627
NM_006939.4(SOS2):c.975T>G (p.Ile325Met) rs2139679163

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