Related gene-specific medical variations for Gene (Select 10105) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3217196	NM_005729.4(PPIF):c.182G>T (p.Arg61Leu)	LOC128462404, PPIF (R61L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570390	NM_005729.4(PPIF):c.520G>A (p.Val174Ile)	LOC128462405, PPIF (V174I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463312	NM_005729.4(PPIF):c.538G>T (p.Val180Phe)	LOC128462405, PPIF (V180F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384887	NM_005729.4(PPIF):c.53G>C (p.Arg18Pro)	LOC128462404, PPIF (R18P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 785321	NM_005729.4(PPIF):c.612C>G (p.Gly204=)	LOC128462405, PPIF	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 728878	NM_005729.4(PPIF):c.561C>T (p.Phe187=)	LOC128462405, PPIF	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar