"PreventionGenetics, part of Exact Sciences"[submitter] AND "PDE10A"[g - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 786541	NM_001385079.1(PDE10A):c.3033C>G (p.Leu1011=)	PDE10A	Single nucleotide variant (synonymous variant)	PDE10A-related disorder +1 more	GBenign
Select item 789513	NM_001385079.1(PDE10A):c.3012T>C (p.Tyr1004=)	PDE10A	Single nucleotide variant (synonymous variant)	PDE10A-related disorder +1 more	GBenign/Likely benign
Select item 810040	NM_001385079.1(PDE10A):c.2896-8C>A	PDE10A	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2630341	NM_001385079.1(PDE10A):c.2828_2829delinsGG (p.Ser943Trp)	PDE10A (S667W +2 more)	Indel (missense variant)	PDE10A-related disorder	GUncertain significance
Select item 2057811	NM_001385079.1(PDE10A):c.2475G>A (p.Ala825=)	PDE10A	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3046675	NM_001385079.1(PDE10A):c.2361G>T (p.Arg787=)	PDE10A	Single nucleotide variant (synonymous variant)	PDE10A-related disorder	GLikely benign
Select item 425404	NM_001385079.1(PDE10A):c.2257C>G (p.Pro753Ala)	PDE10A (P487A +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 723383	NM_001385079.1(PDE10A):c.2085T>C (p.His695=)	PDE10A	Single nucleotide variant (synonymous variant)	PDE10A-related disorder +1 more	GBenign
Select item 1166151	NM_001385079.1(PDE10A):c.1796+9A>T	PDE10A	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 799417	NM_001385079.1(PDE10A):c.1590C>T (p.Leu530=)	PDE10A	Single nucleotide variant (synonymous variant)	PDE10A-related disorder +1 more	GLikely benign
Select item 1122427	NM_001385079.1(PDE10A):c.1371A>G (p.Ser457=)	PDE10A	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2054551	NM_001385079.1(PDE10A):c.1202G>C (p.Cys401Ser)	PDE10A (C135S +2 more)	Single nucleotide variant (missense variant)	PDE10A-related disorder +1 more	GLikely benign
Select item 735881	NM_001385079.1(PDE10A):c.1194+9C>T	PDE10A	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 788415	NM_001385079.1(PDE10A):c.963A>G (p.Lys321=)	PDE10A	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3038031	NM_001385079.1(PDE10A):c.866-32886T>A	PDE10A	Single nucleotide variant (5 prime UTR variant +1 more)	PDE10A-related disorder	GLikely benign