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

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.2792-48T>C	rs540132304	0.00865
NM_005633.4(SOS1):c.2673+14T>C	rs183998234	0.00304
NM_005633.4(SOS1):c.213+16T>C	rs150536159	0.00128
NM_005633.4(SOS1):c.749T>C (p.Val250Ala)	rs139290271	0.00054
NM_005633.4(SOS1):c.2760G>A (p.Arg920=)	rs149092581	0.00051
NM_005633.4(SOS1):c.698A>G (p.Asn233Ser)	rs144934321	0.00026
NM_005633.4(SOS1):c.*4C>T	rs188849286	0.00018
NM_005633.4(SOS1):c.1489C>A (p.Arg497=)	rs542368621	0.00018
NM_005633.4(SOS1):c.109A>G (p.Thr37Ala)	rs150565592	0.00016
NM_005633.4(SOS1):c.1953A>G (p.Pro651=)	rs141507912	0.00013
NM_005633.4(SOS1):c.3600C>G (p.Asp1200Glu)	rs141594736	0.00013
NM_005633.4(SOS1):c.553A>G (p.Ile185Val)	rs143962515	0.00010
NM_005633.4(SOS1):c.2168-50A>C	rs778705378	0.00006
NM_005633.4(SOS1):c.720+9C>T	rs370687707	0.00006
NM_005633.4(SOS1):c.2312T>C (p.Ile771Thr)	rs557328600	0.00005
NM_005633.4(SOS1):c.162A>G (p.Gln54=)	rs763520126	0.00003
NM_005633.4(SOS1):c.2616T>G (p.Leu872=)	rs768058218	0.00003
NM_005633.4(SOS1):c.510+9C>G	rs553448375	0.00003
NM_005633.4(SOS1):c.1008A>G (p.Gln336=)	rs1320092319	0.00002
NM_005633.4(SOS1):c.1202+5A>G	rs1021449471	0.00002
NM_005633.4(SOS1):c.1772A>G (p.Asn591Ser)	rs757213444	0.00002
NM_005633.4(SOS1):c.1203-41C>T	rs568590951	0.00001
NM_005633.4(SOS1):c.1956G>A (p.Glu652=)	rs1365773428	0.00001
NM_005633.4(SOS1):c.2868A>C (p.Ile956=)	rs758834690	0.00001
NM_005633.4(SOS1):c.3060C>T (p.Asn1020=)	rs142431345	0.00001
NM_005633.4(SOS1):c.3552T>G (p.Pro1184=)	rs200485215	0.00001
NM_005633.3(SOS1):c.2511-9dup	rs727503436
NM_005633.4(SOS1):c.2063+44T>C	rs111576630
NM_005633.4(SOS1):c.2511-9del	rs727503436
NM_005633.4(SOS1):c.2674-22C>G	rs61601281
NM_005633.4(SOS1):c.2674-9dup	rs532594344
NM_005633.4(SOS1):c.511-9_511-6del	rs986512473
NM_005633.4(SOS1):c.721-6A>C	rs1671008797

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