List of variants in gene PDE11A reported as uncertain significance for Pigmented nodular adrenocortical disease, primary, 2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_016953.4(PDE11A):c.1655T>C (p.Ile552Thr)	rs138427178	0.00086
NM_016953.4(PDE11A):c.171del (p.Thr58fs)	rs529789124	0.00056
NM_016953.4(PDE11A):c.1973A>G (p.Tyr658Cys)	rs77597060	0.00056
NM_016953.4(PDE11A):c.985C>T (p.Arg329Ter)	rs188985665	0.00042
NM_016953.4(PDE11A):c.2618T>C (p.Ile873Thr)	rs371810618	0.00004
NM_016953.4(PDE11A):c.1774G>A (p.Val592Ile)	rs1307070302	0.00001
NM_016953.4(PDE11A):c.2290C>T (p.Leu764Phe)	rs1323431801	0.00001
NM_016953.4(PDE11A):c.2336T>C (p.Leu779Pro)	rs756779426	0.00001
NM_001077197.2(PDE11A):c.20_21del (p.Arg7fs)	rs202117698
NM_016953.4(PDE11A):c.126_127del (p.His42fs)
NM_016953.4(PDE11A):c.1660del (p.Cys554fs)	rs573163079
NM_016953.4(PDE11A):c.2044A>G (p.Thr682Ala)
NM_016953.4(PDE11A):c.2422C>T (p.Arg808Ter)
NM_016953.4(PDE11A):c.2436G>A (p.Met812Ile)
NM_016953.4(PDE11A):c.2678C>A (p.Pro893Gln)	rs200504859
NM_016953.4(PDE11A):c.493C>A (p.Pro165Thr)	rs779068288
Single allele

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