List of variants reported as likely benign for obsolete Noonan-like/multiple giant cell lesion syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
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.2673+14T>C	rs183998234	0.00304
NM_005633.4(SOS1):c.570C>T (p.Asp190=)	rs55980502	0.00233
NM_005633.4(SOS1):c.3081+13A>G	rs189695571	0.00223
NM_005633.4(SOS1):c.3032A>G (p.Asn1011Ser)	rs8192671	0.00164
NM_005633.4(SOS1):c.2238T>C (p.Asn746=)	rs75877625	0.00084
NM_005633.4(SOS1):c.73C>T (p.Pro25Ser)	rs139592595	0.00082
NM_005633.4(SOS1):c.3357C>T (p.Thr1119=)	rs373319212	0.00011
NM_005633.4(SOS1):c.1490G>A (p.Arg497Gln)	rs371314838	0.00004
NM_005633.4(SOS1):c.1905C>T (p.Cys635=)	rs762900789	0.00004
NM_005633.4(SOS1):c.1848T>C (p.His616=)	rs1344852617	0.00001
NM_005633.4(SOS1):c.2604T>C (p.Phe868=)	rs756520305	0.00001
NM_005633.4(SOS1):c.984C>T (p.Gly328=)	rs778223456	0.00001
NM_005633.4(SOS1):c.2674-9dup	rs532594344

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