"St. Jude Molecular Pathology, St. Jude Children's Research Hospital"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1710960	NM_006939.4(SOS2):c.3965T>C (p.Leu1322Pro)	SOS2 (L1289P +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2444865	NM_006939.4(SOS2):c.3604A>G (p.Ser1202Gly)	SOS2 (S1169G +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 579913	NM_006939.4(SOS2):c.3403A>G (p.Ser1135Gly)	SOS2 (S1135G)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GUncertain significance
Select item 862440	NM_006939.4(SOS2):c.3289T>C (p.Ser1097Pro)	SOS2 (S1097P)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 1691536	NM_006939.4(SOS2):c.2182G>A (p.Val728Ile)	SOS2 (V728I)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1691522	NM_006939.4(SOS2):c.1973A>G (p.Lys658Arg)	SOS2 (K658R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 542401	NM_006939.4(SOS2):c.1868G>A (p.Arg623His)	SOS2 (R623H)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2444872	NM_006939.4(SOS2):c.1209C>A (p.Cys403Ter)	SOS2 (C370* +1 more)	Single nucleotide variant (nonsense)	Noonan syndrome 9	GUncertain significance

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