"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PDE1C"[ - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 709900	NM_001191057.4(PDE1C):c.1979G>A (p.Arg660His)	PDE1C (R660H +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 773211	NM_001191057.4(PDE1C):c.1953G>C (p.Thr651=)	PDE1C	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 789008	NM_001191057.4(PDE1C):c.1904G>A (p.Arg635His)	PDE1C (R635H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 740251	NM_001191057.4(PDE1C):c.1866C>T (p.Ile622=)	PDE1C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 773889	NM_001191057.4(PDE1C):c.1726G>C (p.Val576Leu)	PDE1C (V711L +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1518318	NM_001191057.4(PDE1C):c.1076C>T (p.Pro359Leu)	PDE1C (P359L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 708869	NM_001191057.4(PDE1C):c.525C>T (p.Ser175=)	PDE1C	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 724139	NM_001191057.4(PDE1C):c.366C>T (p.Asp122=)	PDE1C	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778019	NM_001191058.4(PDE1C):c.279C>T (p.Ser93=)	PDE1C	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 776215	NM_001191058.4(PDE1C):c.160T>A (p.Trp54Arg)	PDE1C (W54R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign