"CLPX-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040415	NM_006660.5(CLPX):c.*6C>T	CLPX	Single nucleotide variant (3 prime UTR variant +1 more)	CLPX-related condition	GLikely benign
Select item 1603579	NM_006660.5(CLPX):c.1398G>A (p.Ser466=)	CLPX	Single nucleotide variant (synonymous variant +1 more)	CLPX-related condition +1 more	GBenign/Likely benign
Select item 1652180	NM_006660.5(CLPX):c.893-8A>G	CLPX	Single nucleotide variant (intron variant)	CLPX-related condition +1 more	GLikely benign
Select item 1600204	NM_006660.5(CLPX):c.748G>A (p.Gly250Ser)	CLPX (G250S)	Single nucleotide variant (missense variant +1 more)	CLPX-related condition +1 more	GBenign
Select item 1645480	NM_006660.5(CLPX):c.137C>T (p.Thr46Ile)	CLPX (T46I)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2069220	NM_006660.5(CLPX):c.42C>T (p.Val14=)	CLPX	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign

ClinVar