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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 226522	NM_006012.4(CLPP):c.-5G>A	CLPP	Single nucleotide variant (5 prime UTR variant)	not specified +2 more	GBenign
Select item 559365	NM_006012.4(CLPP):c.216C>T (p.Ala72=)	CLPP, LOC130063288	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 226519	NM_006012.4(CLPP):c.368-8G>A	CLPP	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 226520	NM_006012.4(CLPP):c.405G>A (p.Thr135=)	CLPP	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 504859	NM_006012.4(CLPP):c.667G>A (p.Ala223Thr)	CLPP (A223T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 226523	NM_006012.4(CLPP):c.801G>A (p.Ala267=)	CLPP	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

ClinVar