"Ambry Genetics"[submitter] AND "LOC129936929"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3210635	NM_177966.7(PDE12):c.704A>G (p.Tyr235Cys)	LOC129936929, PDE12 (Y235C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210636	NM_177966.7(PDE12):c.728G>C (p.Gly243Ala)	LOC129936929, PDE12 (G243A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210637	NM_177966.7(PDE12):c.760G>A (p.Asp254Asn)	LOC129936929, PDE12 (D254N)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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ClinVar