List of variants in gene SOS1 reported as pathogenic by Ambry Genetics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.1132A>G (p.Thr378Ala)	rs397517146
NM_005633.4(SOS1):c.1300G>A (p.Gly434Arg)	rs397517148
NM_005633.4(SOS1):c.1310T>C (p.Ile437Thr)	rs397517150
NM_005633.4(SOS1):c.1642A>C (p.Ser548Arg)	rs397517149
NM_005633.4(SOS1):c.1654A>G (p.Arg552Gly)	rs137852814
NM_005633.4(SOS1):c.1655G>C (p.Arg552Thr)	rs397517154
NM_005633.4(SOS1):c.1656G>T (p.Arg552Ser)	rs267607079
NM_005633.4(SOS1):c.2536G>A (p.Glu846Lys)	rs397517159
NM_005633.4(SOS1):c.508A>G (p.Lys170Glu)	rs397517172
NM_005633.4(SOS1):c.806T>C (p.Met269Thr)	rs137852813
NM_005633.4(SOS1):c.806T>G (p.Met269Arg)	rs137852813

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