"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "ZAP70"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2682740	NM_001079.4(ZAP70):c.197A>G (p.Asn66Ser)	ZAP70 (N66S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 939404	NM_001079.4(ZAP70):c.474C>G (p.His158Gln)	ZAP70 (H158Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 337634	NM_001079.4(ZAP70):c.1025T>C (p.Ile342Thr)	ZAP70 (I342T +1 more)	Single nucleotide variant (missense variant)	ZAP70-Related Severe Combined Immunodeficiency +3 more	GConflicting classifications of pathogenicity
Select item 538573	NM_001079.4(ZAP70):c.1289+10G>A	ZAP70	Single nucleotide variant (intron variant)	ZAP70-Related Severe Combined Immunodeficiency +2 more	GConflicting classifications of pathogenicity
Select item 650235	NM_001079.4(ZAP70):c.1556G>A (p.Arg519His)	ZAP70 (R212H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 337637	NM_001079.4(ZAP70):c.1645A>G (p.Met549Val)	ZAP70 (M549V +1 more)	Single nucleotide variant (missense variant)	Autoimmune disease, multisystem, infantile-onset, 2 +4 more	GUncertain significance

ClinVar