"PreventionGenetics, part of Exact Sciences"[submitter] AND "KCND3"[ge - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 519434	NM_001378969.1(KCND3):c.1573A>G (p.Met525Val)	KCND3 (M525V +1 more)	Single nucleotide variant (missense variant)	KCND3-related disorder +4 more	GBenign/Likely benign
Select item 415286	NM_001378969.1(KCND3):c.1456A>G (p.Thr486Ala)	KCND3 (T486A)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 3052055	NM_001378969.1(KCND3):c.1389G>A (p.Glu463=)	KCND3	Single nucleotide variant (synonymous variant)	KCND3-related disorder	GLikely benign
Select item 510916	NM_001378969.1(KCND3):c.1359G>A (p.Ala453=)	KCND3	Single nucleotide variant (synonymous variant)	KCND3-related disorder +3 more	GLikely benign
Select item 447626	NM_001378969.1(KCND3):c.1354G>A (p.Glu452Lys)	KCND3 (E452K)	Single nucleotide variant (missense variant)	Primary dilated cardiomyopathy +5 more	GBenign/Likely benign
Select item 259600	NM_001378969.1(KCND3):c.1269+15C>A	KCND3	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1577729	NM_001378969.1(KCND3):c.324C>T (p.Tyr108=)	KCND3	Single nucleotide variant (synonymous variant)	KCND3-related disorder +2 more	GLikely benign
Select item 129314	NM_001378969.1(KCND3):c.264C>T (p.Pro88=)	KCND3	Single nucleotide variant (synonymous variant)	Spinocerebellar ataxia type 19/22 +2 more	GBenign
Select item 586065	NM_001378969.1(KCND3):c.207G>A (p.Thr69=)	KCND3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 1782277	NM_001378969.1(KCND3):c.18G>A (p.Ala6=)	KCND3	Single nucleotide variant (synonymous variant)	Spinocerebellar ataxia type 19/22 +2 more	GLikely benign