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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3379503	NM_000096.4(CP):c.2989C>T (p.His997Tyr)	CP (H997Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2192691	NM_000096.4(CP):c.2741T>G (p.Leu914Arg)	CP (L914R)	Single nucleotide variant (missense variant +1 more)	Deficiency of ferroxidase +1 more	GUncertain significance
Select item 3379505	NM_000096.4(CP):c.2407_2409delinsCAT (p.Glu803His)	CP (E803H)	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 343773	NM_000096.4(CP):c.1217C>A (p.Ala406Glu)	CP (A406E)	Single nucleotide variant (missense variant +1 more)	Deficiency of ferroxidase +2 more	GConflicting classifications of pathogenicity
Select item 3379506	NM_000096.4(CP):c.1174A>T (p.Ile392Phe)	CP (I392F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3379507	NM_000096.4(CP):c.1100G>A (p.Arg367His)	CP (R367H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 343779	NM_000096.4(CP):c.938C>T (p.Thr313Ile)	CP (T313I)	Single nucleotide variant (missense variant +1 more)	Deficiency of ferroxidase +2 more	GConflicting classifications of pathogenicity
Select item 2157586	NM_000096.4(CP):c.181G>T (p.Asp61Tyr)	CP (D61Y)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

ClinVar