C1864851[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2434620	NM_016953.4(PDE11A):c.2422C>T (p.Arg808Ter)	PDE11A, PDE11A-AS1 (R364* +3 more)	Single nucleotide variant (nonsense)	Pigmented nodular adrenocortical disease, primary, 2	GUncertain significance
Select item 2434619	NM_016953.4(PDE11A):c.2044A>G (p.Thr682Ala)	PDE11A, PDE11A-AS1 (T238A +3 more)	Single nucleotide variant (missense variant)	Pigmented nodular adrenocortical disease, primary, 2	GUncertain significance
Select item 1324868	NM_016953.4(PDE11A):c.1585C>T (p.Gln529Ter)	PDE11A (Q171* +3 more)	Single nucleotide variant (nonsense)	Pigmented nodular adrenocortical disease, primary, 2	GLikely pathogenic
Select item 1324867	NM_016953.4(PDE11A):c.1270_1280del (p.Ser424fs)	PDE11A (S174fs +2 more)	Deletion (frameshift variant)	Pigmented nodular adrenocortical disease, primary, 2	GLikely pathogenic
Select item 2432520	NM_016953.4(PDE11A):c.1149T>A (p.Tyr383Ter)	PDE11A (Y133* +2 more)	Single nucleotide variant (nonsense)	Pigmented nodular adrenocortical disease, primary, 2	GLikely pathogenic
Select item 2432528	NM_016953.4(PDE11A):c.126_127del (p.His42fs)	PDE11A (H42fs)	Microsatellite (frameshift variant +1 more)	Pigmented nodular adrenocortical disease, primary, 2	GUncertain significance

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