ClinVar for MedGen (Select 1794237) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3067997	NM_014550.4(CARD10):c.863A>C (p.Gln288Pro)	CARD10 (Q288P)	Single nucleotide variant (missense variant)	Immunodeficiency 89 and autoimmunity	GUncertain significance
Select item 2664195	NM_014550.4(CARD10):c.1307C>T (p.Thr436Met)	CARD10 (T436M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1326845	NM_014550.4(CARD10):c.1258C>T (p.Arg420Cys)	CARD10 (R420C)	Single nucleotide variant (missense variant)	Immunodeficiency 89 and autoimmunity	GPathogenic

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