"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PDE2A"[gen - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2642122	NM_002599.5(PDE2A):c.2688C>A (p.Thr896=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642123	NM_002599.5(PDE2A):c.2277T>C (p.Asp759=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2176745	NM_002599.5(PDE2A):c.2182-4C>G	PDE2A	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity
Select item 1615142	NM_002599.5(PDE2A):c.1980C>T (p.His660=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1621394	NM_002599.5(PDE2A):c.1785C>T (p.Ala595=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642124	NM_002599.5(PDE2A):c.1449C>G (p.Ala483=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1335080	NM_002599.5(PDE2A):c.1398G>A (p.Ala466=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1594977	NM_002599.5(PDE2A):c.1341G>C (p.Gly447=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1424027	NM_002599.5(PDE2A):c.939C>T (p.Ser313=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 1175802	NM_002599.5(PDE2A):c.676C>T (p.Arg226Cys)	PDE2A (R205C +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1298521	NM_002599.5(PDE2A):c.624C>T (p.Asn208=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642125	NM_002599.5(PDE2A):c.606T>A (p.Ala202=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642126	NM_002599.5(PDE2A):c.528C>A (p.Ser176Arg)	PDE2A (S155R +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1653974	NM_002599.5(PDE2A):c.447G>A (p.Pro149=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642127	NM_002599.5(PDE2A):c.300G>A (p.Glu100=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642128	NM_002599.5(PDE2A):c.225C>G (p.Leu75=)	PDE2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign