"PreventionGenetics, part of Exact Sciences"[submitter] AND "KCTD1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1243729	NM_001142730.3(KCTD1):c.2517C>T (p.Ser839=)	KCTD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2175670	NM_001142730.3(KCTD1):c.2133+4A>G	KCTD1	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3042305	NM_001142730.3(KCTD1):c.1791T>C (p.Ala597=)	KCTD1	Single nucleotide variant (synonymous variant +1 more)	KCTD1-related disorder	GLikely benign
Select item 3035828	NM_001142730.3(KCTD1):c.1623C>T (p.Phe541=)	KCTD1	Single nucleotide variant (synonymous variant +1 more)	KCTD1-related disorder	GLikely benign
Select item 3029434	NM_001142730.3(KCTD1):c.1296C>T (p.Gly432=)	KCTD1	Single nucleotide variant (synonymous variant +1 more)	KCTD1-related disorder	GLikely benign
Select item 2635088	NM_001142730.3(KCTD1):c.815A>G (p.Glu272Gly)	KCTD1 (E272G)	Single nucleotide variant (missense variant +1 more)	KCTD1-related disorder	GUncertain significance
Select item 3041725	NM_001142730.3(KCTD1):c.54C>T (p.Ala18=)	KCTD1	Single nucleotide variant (synonymous variant +1 more)	KCTD1-related disorder	GLikely benign

ClinVar