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

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 883645	NM_001920.5(DCN):c.1066G>A (p.Gly356Arg)	DCN (G169R +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2616989	NM_001920.5(DCN):c.1048C>T (p.Arg350Cys)	DCN (R203C +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2302363	NM_001920.5(DCN):c.1045G>A (p.Val349Met)	DCN (V162M +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2245169	NM_001920.5(DCN):c.1033A>G (p.Arg345Gly)	DCN (R158G +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2609572	NM_001920.5(DCN):c.1014G>C (p.Glu338Asp)	DCN (E151D +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2908085	NM_001920.5(DCN):c.959A>G (p.Lys320Arg)	DCN (K211R +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2542060	NM_001920.5(DCN):c.941C>T (p.Pro314Leu)	DCN (P127L +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3080556	NM_001920.5(DCN):c.878A>G (p.Tyr293Cys)	DCN (Y146C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3271099	NM_001920.5(DCN):c.865G>A (p.Ala289Thr)	DCN (A142T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2225443	NM_001920.5(DCN):c.697A>G (p.Ile233Val)	DCN (I124V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 881297	NM_001920.5(DCN):c.671C>T (p.Thr224Met)	DCN (T77M +2 more)	Single nucleotide variant (missense variant +1 more)	Congenital stromal corneal dystrophy +1 more	GConflicting classifications of pathogenicity
Select item 2616108	NM_001920.5(DCN):c.658C>T (p.Pro220Ser)	DCN (P111S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2486596	NM_001920.5(DCN):c.638C>T (p.Thr213Ile)	DCN (T104I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2607693	NM_001920.5(DCN):c.554C>T (p.Pro185Leu)	DCN (P76L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3271096	NM_001920.5(DCN):c.512A>G (p.Asn171Ser)	DCN (N171S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3271098	NM_001920.5(DCN):c.510C>G (p.Phe170Leu)	DCN (F170L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2494705	NM_001920.5(DCN):c.437A>G (p.Glu146Gly)	DCN (E146G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3271097	NM_001920.5(DCN):c.385G>A (p.Val129Met)	DCN (V129M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2304904	NM_001920.5(DCN):c.233A>T (p.Asp78Val)	DCN (D78V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3080555	NM_001920.5(DCN):c.142C>A (p.Pro48Thr)	DCN (P48T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232169	NM_001920.5(DCN):c.130C>G (p.Arg44Gly)	DCN (R44G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2402806	NM_001920.5(DCN):c.92A>G (p.Asp31Gly)	DCN (D31G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220822	NM_001920.5(DCN):c.10A>G (p.Thr4Ala)	DCN (T4A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 23