"Ambry Genetics"[submitter] AND "DCTD"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2385411	NM_001921.3(DCTD):c.528G>C (p.Lys176Asn)	DCTD (K187N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593953	NM_001921.3(DCTD):c.518C>T (p.Pro173Leu)	DCTD (P173L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2230544	NM_001921.3(DCTD):c.497T>G (p.Phe166Cys)	DCTD (F166C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2318549	NM_001921.3(DCTD):c.409G>A (p.Glu137Lys)	DCTD (E137K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2246847	NM_001921.3(DCTD):c.291T>A (p.Asp97Glu)	DCTD (D108E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2276350	NM_001921.3(DCTD):c.181A>T (p.Ser61Cys)	DCTD (S61C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618383	NM_001921.3(DCTD):c.148G>T (p.Gly50Trp)	DCTD (G61W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2244755	NM_001921.3(DCTD):c.68C>G (p.Ala23Gly)	DCTD (A34G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar