ClinVar Miner

List of variants in gene SOS2 reported as uncertain significance for not provided

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Total variants: 21
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HGVS dbSNP
NM_006939.4(SOS2):c.1175A>G (p.Tyr392Cys) rs1085307558
NM_006939.4(SOS2):c.1273A>G (p.Lys425Glu) rs372203654
NM_006939.4(SOS2):c.142A>G (p.Ile48Val) rs763552267
NM_006939.4(SOS2):c.1550A>G (p.Lys517Arg) rs367970301
NM_006939.4(SOS2):c.1861T>G (p.Phe621Val) rs1555370029
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.2443A>G (p.Asn815Asp) rs886041958
NM_006939.4(SOS2):c.2843A>G (p.Lys948Arg)
NM_006939.4(SOS2):c.2978A>T (p.Asn993Ile) rs776000121
NM_006939.4(SOS2):c.3076C>T (p.Pro1026Ser) rs201874067
NM_006939.4(SOS2):c.322G>A (p.Asp108Asn) rs1566477432
NM_006939.4(SOS2):c.3235A>G (p.Thr1079Ala) rs61755576
NM_006939.4(SOS2):c.3379+1G>C rs1566818889
NM_006939.4(SOS2):c.3584C>T (p.Ala1195Val) rs753151750
NM_006939.4(SOS2):c.3755_3757del (p.Ile1252del) rs775506222
NM_006939.4(SOS2):c.3968C>T (p.Pro1323Leu) rs886041929
NM_006939.4(SOS2):c.536A>G (p.Asp179Gly) rs770997822
NM_006939.4(SOS2):c.572C>T (p.Pro191Leu) rs72681869
NM_006939.4(SOS2):c.842T>C (p.Phe281Ser) rs1555371627
NM_006939.4(SOS2):c.973A>T (p.Ile325Phe) rs1594993511

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