ClinVar Miner

List of variants in gene SOS1 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
GRCh38/hg38 2p22.1(chr2:39097156-39101653)x1
NM_005633.3(SOS1):c.*4C>T rs188849286
NM_005633.3(SOS1):c.-47C>G rs201218035
NM_005633.3(SOS1):c.-9G>A rs587781175
NM_005633.3(SOS1):c.1074+285G>A
NM_005633.3(SOS1):c.1074+5G>C rs145155424
NM_005633.3(SOS1):c.1203-20T>C rs112906251
NM_005633.3(SOS1):c.1203-307T>C
NM_005633.3(SOS1):c.1566T>C (p.Asn522=) rs145325119
NM_005633.3(SOS1):c.1647A>G (p.Thr549=) rs139683425
NM_005633.3(SOS1):c.1772A>G (p.Asn591Ser) rs757213444
NM_005633.3(SOS1):c.1858+142A>G
NM_005633.3(SOS1):c.1858+302G>C
NM_005633.3(SOS1):c.1941-44C>T
NM_005633.3(SOS1):c.1953A>G (p.Pro651=) rs141507912
NM_005633.3(SOS1):c.1962G>A (p.Glu654=) rs144382701
NM_005633.3(SOS1):c.1989A>C (p.Ile663=) rs587781172
NM_005633.3(SOS1):c.213+16T>C rs150536159
NM_005633.3(SOS1):c.2167+6T>G rs186640807
NM_005633.3(SOS1):c.2238T>C (p.Asn746=) rs75877625
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.3(SOS1):c.2511-301_2511-300insCT rs5830552
NM_005633.3(SOS1):c.2673+14T>C rs183998234
NM_005633.3(SOS1):c.2760G>A (p.Arg920=) rs149092581
NM_005633.3(SOS1):c.2964+17A>G rs201906525
NM_005633.3(SOS1):c.3032A>G (p.Asn1011Ser) rs8192671
NM_005633.3(SOS1):c.3081+13A>G rs189695571
NM_005633.3(SOS1):c.3081+32A>G rs6723430
NM_005633.3(SOS1):c.3347-243delT rs5830550
NM_005633.3(SOS1):c.3347-318A>G
NM_005633.3(SOS1):c.3391+7A>G rs201982464
NM_005633.3(SOS1):c.345+12_345+13dupCT rs397517167
NM_005633.3(SOS1):c.345+15C>T rs75937422
NM_005633.3(SOS1):c.345+259_345+262delGTTT rs148203100
NM_005633.3(SOS1):c.3585A>G (p.Arg1195=) rs587781173
NM_005633.3(SOS1):c.864+219G>A
NM_005633.3:c.1-36_1-34delGCC

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