ClinVar Miner

List of variants in gene SOS2 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP
NM_006939.4(SOS2):c.1068+106T>C rs536957409
NM_006939.4(SOS2):c.1068+114_1068+117del rs34333845
NM_006939.4(SOS2):c.1068+256TA[3] rs35893256
NM_006939.4(SOS2):c.1069-154G>T rs12717405
NM_006939.4(SOS2):c.1196+252G>A rs7154198
NM_006939.4(SOS2):c.1196+266C>T rs7154516
NM_006939.4(SOS2):c.1197-121_1197-119del rs60130456
NM_006939.4(SOS2):c.1197-32G>A rs4900992
NM_006939.4(SOS2):c.1263T>C (p.Asn421=) rs369267864
NM_006939.4(SOS2):c.1344G>A (p.Leu448=) rs35530861
NM_006939.4(SOS2):c.1448G>A (p.Ser483Asn) rs17122201
NM_006939.4(SOS2):c.1852+174A>G rs10483598
NM_006939.4(SOS2):c.1852+285G>A rs61093617
NM_006939.4(SOS2):c.2014C>A (p.Leu672Ile) rs34139502
NM_006939.4(SOS2):c.2057+273G>A rs17122199
NM_006939.4(SOS2):c.2057+288dup rs139321261
NM_006939.4(SOS2):c.2058-36T>C rs11628935
NM_006939.4(SOS2):c.2058-71G>A rs117064591
NM_006939.4(SOS2):c.213+18A>T rs143888968
NM_006939.4(SOS2):c.213+37C>G rs1075537
NM_006939.4(SOS2):c.214-265C>T rs12882042
NM_006939.4(SOS2):c.2162-4C>A rs57179949
NM_006939.4(SOS2):c.2232C>T (p.Asn744=) rs2229869
NM_006939.4(SOS2):c.2385-100G>A rs726797
NM_006939.4(SOS2):c.2385-143G>A rs726798
NM_006939.4(SOS2):c.2385-87A>G rs1014879
NM_006939.4(SOS2):c.2520A>G (p.Ala840=) rs775682587
NM_006939.4(SOS2):c.2667+43G>A rs2064667
NM_006939.4(SOS2):c.2668-120T>C rs2024808
NM_006939.4(SOS2):c.2668-4T>C rs763298498
NM_006939.4(SOS2):c.2785+226A>G rs12892681
NM_006939.4(SOS2):c.2785+276T>C rs7154299
NM_006939.4(SOS2):c.2785+44T>C rs17122174
NM_006939.4(SOS2):c.2958+172G>A rs7147778
NM_006939.4(SOS2):c.2958+209G>A rs142022441
NM_006939.4(SOS2):c.2959-121G>A rs12882504
NM_006939.4(SOS2):c.2959-38T>A rs28565912
NM_006939.4(SOS2):c.3075+7C>T rs144391749
NM_006939.4(SOS2):c.3337+207A>G rs1955930
NM_006939.4(SOS2):c.3338-142A>G rs3759597
NM_006939.4(SOS2):c.3380-239A>G rs78111482
NM_006939.4(SOS2):c.345+145C>T rs6572648
NM_006939.4(SOS2):c.3489+19C>T rs149825446
NM_006939.4(SOS2):c.3490-18A>C rs79858475
NM_006939.4(SOS2):c.3490-294T>C rs7156414
NM_006939.4(SOS2):c.3813G>A (p.Pro1271=) rs2227276
NM_006939.4(SOS2):c.510+146G>A rs1955924
NM_006939.4(SOS2):c.549G>C (p.Leu183Phe) rs137961578
NM_006939.4(SOS2):c.572C>G (p.Pro191Arg) rs72681869
NM_006939.4(SOS2):c.591A>G (p.Leu197=) rs113460230
NM_006939.4(SOS2):c.622G>A (p.Ala208Thr) rs61755579
NM_006939.4(SOS2):c.714+266G>A rs7157329
NM_006939.4(SOS2):c.714+294C>T rs12894390
NM_006939.4(SOS2):c.714+65_714+68del rs67021603
NM_006939.4(SOS2):c.816T>C (p.Ser272=) rs35396088
NM_006939.4(SOS2):c.858+174_858+175insGGACTGCTTG rs111808923
NM_006939.4(SOS2):c.858+93G>A rs2024811
NM_006939.4(SOS2):c.858+9A>G rs201701595
NM_006939.4(SOS2):c.859-123A>G rs73289621
NM_006939.4(SOS2):c.859-152G>A rs28452354
NM_006939.4(SOS2):c.859-259C>T rs17715073
NM_006939.4(SOS2):c.859-90C>T rs28734119
NM_006939.4(SOS2):c.87+37G>A rs2273326
NM_006939.4(SOS2):c.88-6T>C rs12888783
NM_006939.4(SOS2):c.970-107T>C rs73285531
NM_006939.4(SOS2):c.970-194C>G rs79843008
NM_006939.4(SOS2):c.970-77A>C rs10782418

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