List of variants in gene SOS1 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.2964+43C>A	rs1454223	0.94284
NM_005633.4(SOS1):c.720+25C>G	rs997344	0.92897
NM_005633.4(SOS1):c.195A>C (p.Arg65=)	rs7609455	0.03809
NM_005633.4(SOS1):c.3081+32A>G	rs6723430	0.02350
NM_005633.4(SOS1):c.1203-20T>C	rs112906251	0.01058
NM_005633.4(SOS1):c.1964C>T (p.Pro655Leu)	rs56219475	0.00787
NM_005633.4(SOS1):c.1074+5G>C	rs145155424	0.00655
NM_005633.4(SOS1):c.345+15C>T	rs75937422	0.00407
NM_005633.4(SOS1):c.2997T>C (p.Asn999=)	rs145364368	0.00352
NM_005633.4(SOS1):c.2122G>A (p.Ala708Thr)	rs140811086	0.00280
NM_005633.4(SOS1):c.3081+13A>G	rs189695571	0.00223
NM_005633.4(SOS1):c.1230G>A (p.Gln410=)	rs141390073	0.00217
NM_005633.4(SOS1):c.3032A>G (p.Asn1011Ser)	rs8192671	0.00164
NM_005633.4(SOS1):c.2988G>A (p.Pro996=)	rs35462677	0.00156
NM_005633.4(SOS1):c.3391+7A>G	rs201982464	0.00066
NM_005633.4(SOS1):c.1705C>G (p.Leu569Val)	rs200786705	0.00019
NM_005633.4(SOS1):c.1018C>T (p.Pro340Ser)	rs190222208	0.00006
NM_005633.4(SOS1):c.2792-50dup	rs869215095

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