"PreventionGenetics, part of Exact Sciences"[submitter] AND "CACNA2D3- - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3037580	NM_018398.3(CACNA2D3):c.1783-10_1783-9del	CACNA2D3, CACNA2D3-AS1	Deletion (intron variant)	CACNA2D3-related condition	GBenign
Select item 2635505	NM_018398.3(CACNA2D3):c.1870C>A (p.His624Asn)	CACNA2D3, CACNA2D3-AS1 (H624N)	Single nucleotide variant (missense variant)	CACNA2D3-related condition	GUncertain significance
Select item 3053454	NM_018398.3(CACNA2D3):c.2091C>T (p.Asp697=)	CACNA2D3, CACNA2D3-AS1	Single nucleotide variant (synonymous variant)	CACNA2D3-related condition	GLikely benign
Select item 2633138	NM_018398.3(CACNA2D3):c.2104G>A (p.Ala702Thr)	CACNA2D3, CACNA2D3-AS1 (A702T)	Single nucleotide variant (missense variant)	CACNA2D3-related condition	GUncertain significance
Select item 773444	NM_018398.3(CACNA2D3):c.2195C>T (p.Thr732Met)	CACNA2D3-AS1, CACNA2D3 (T732M)	Single nucleotide variant (missense variant)	CACNA2D3-related condition +1 more	GBenign
Select item 3058065	NM_018398.3(CACNA2D3):c.2286C>T (p.Asn762=)	CACNA2D3, CACNA2D3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	CACNA2D3-related condition	GLikely benign
Select item 3030915	NM_018398.3(CACNA2D3):c.2293C>T (p.His765Tyr)	CACNA2D3, CACNA2D3-AS1 (H765Y)	Single nucleotide variant (non-coding transcript variant +1 more)	CACNA2D3-related condition	GUncertain significance
Select item 3038777	NM_018398.3(CACNA2D3):c.2426A>G (p.Glu809Gly)	CACNA2D3, CACNA2D3-AS1 (E809G)	Single nucleotide variant (missense variant)	CACNA2D3-related condition	GLikely benign