"PRODH2-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052785	NM_021232.2(PRODH2):c.1001+8C>T	PRODH2	Single nucleotide variant (intron variant)	PRODH2-related disorder	GLikely benign
Select item 3047491	NM_021232.2(PRODH2):c.686G>A (p.Arg229Gln)	PRODH2 (R229Q)	Single nucleotide variant (missense variant +1 more)	PRODH2-related disorder	GLikely benign
Select item 3056564	NM_021232.2(PRODH2):c.599A>G (p.Asn200Ser)	PRODH2 (N200S)	Single nucleotide variant (missense variant)	PRODH2-related disorder	GBenign
Select item 3037535	NM_021232.2(PRODH2):c.590C>G (p.Ser197Cys)	PRODH2 (S197C)	Single nucleotide variant (missense variant)	PRODH2-related disorder	GLikely benign
Select item 3047438	NM_021232.2(PRODH2):c.-29C>T	PRODH2	Single nucleotide variant (5 prime UTR variant)	PRODH2-related disorder	GLikely benign
Select item 3053337	NM_021232.1(PRODH2):c.104C>T (p.Ala35Val)	PRODH2 (A35V)	Single nucleotide variant (missense variant)	PRODH2-related disorder	GLikely benign
Select item 3041011	NM_021232.1(PRODH2):c.72C>T (p.Thr24=)	PRODH2	Single nucleotide variant (synonymous variant)	PRODH2-related disorder	GLikely benign

ClinVar