"Ambry Genetics"[submitter] AND "LOC129936928"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2515191	NM_177966.7(PDE12):c.31C>T (p.Leu11Phe)	LOC129936928, PDE12 (L11F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258317	NM_177966.7(PDE12):c.101C>T (p.Ala34Val)	LOC129936928, PDE12 (A34V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305344	NM_177966.7(PDE12):c.127G>C (p.Val43Leu)	LOC129936928, PDE12 (V43L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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ClinVar