"Ambry Genetics"[submitter] AND "PRDX5"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2513977	NM_012094.5(PRDX5):c.49C>A (p.Leu17Ile)	PRDX5, TRMT112 (L17I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2303661	NM_012094.5(PRDX5):c.55G>C (p.Gly19Arg)	PRDX5, TRMT112 (G19R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2338410	NM_012094.5(PRDX5):c.274G>C (p.Val92Leu)	PRDX5 (V40L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2346306	NM_012094.5(PRDX5):c.469T>G (p.Phe157Val)	PRDX5 (F105V +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2278467	NM_012094.5(PRDX5):c.527G>A (p.Arg176Gln)	PRDX5 (R176Q +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548275	NM_012094.5(PRDX5):c.549G>A (p.Met183Ile)	PRDX5 (M131I +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2469131	NM_012094.5(PRDX5):c.613A>G (p.Ser205Gly)	PRDX5 (S153G +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar