List of variants in gene SOS1 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.2791+53C>T	rs7577088	0.94549
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.2167+6T>G	rs186640807	0.00510
NM_005633.4(SOS1):c.2673+14T>C	rs183998234	0.00304
NM_005633.4(SOS1):c.3081+26G>A	rs186106971	0.00284
NM_005633.4(SOS1):c.2122G>A (p.Ala708Thr)	rs140811086	0.00280
NM_005633.4(SOS1):c.570C>T (p.Asp190=)	rs55980502	0.00233
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.3347-20T>G	rs727505382	0.00001
NM_005633.3:c.213+15C>G
NM_005633.4(SOS1):c.2167+16dup	rs79984786
NM_005633.4(SOS1):c.2964+32T>G	rs727505384

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