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

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2269195	NM_001372108.2(DDO):c.1000A>G (p.Thr334Ala)	DDO (T221A +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2472476	NM_001372108.2(DDO):c.928G>T (p.Gly310Cys)	DDO (G197C +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080804	NM_001372108.2(DDO):c.914G>C (p.Gly305Ala)	DDO (G192A +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080803	NM_001372108.2(DDO):c.883G>A (p.Gly295Arg)	DDO (G177R +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080801	NM_001372108.2(DDO):c.689A>G (p.His230Arg)	DDO (H117R +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080800	NM_001372108.2(DDO):c.668A>G (p.Tyr223Cys)	DDO (Y110C +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3271213	NM_001372108.2(DDO):c.622G>C (p.Ala208Pro)	DDO (A90P +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2266442	NM_001372108.2(DDO):c.593C>T (p.Pro198Leu)	DDO (P144L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406225	NM_001372108.2(DDO):c.575G>A (p.Gly192Glu)	DDO (G133E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080798	NM_001372108.2(DDO):c.567G>C (p.Gln189His)	DDO (Q130H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080797	NM_001372108.2(DDO):c.535G>A (p.Val179Met)	DDO (V61M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080796	NM_001372108.2(DDO):c.488C>T (p.Thr163Ile)	DDO (T50I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3271216	NM_001372108.2(DDO):c.434C>T (p.Ala145Val)	DDO (A145V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3271214	NM_001372108.2(DDO):c.403G>A (p.Ala135Thr)	DDO (A81T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623911	NM_001372108.2(DDO):c.392T>G (p.Val131Gly)	DDO (V13G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3271212	NM_001372108.2(DDO):c.367G>A (p.Glu123Lys)	DDO (E5K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080795	NM_001372108.2(DDO):c.356T>C (p.Met119Thr)	DDO (M119T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2218677	NM_001372108.2(DDO):c.356T>G (p.Met119Arg)	DDO (M119R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3271211	NM_001372108.2(DDO):c.305C>T (p.Pro102Leu)	DDO (P48L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080794	NM_001372108.2(DDO):c.268C>T (p.His90Tyr)	DDO (H36Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2604905	NM_001372108.2(DDO):c.257A>T (p.Asp86Val)	DDO (D86V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080793	NM_001372108.2(DDO):c.223C>T (p.Leu75Phe)	DDO (L75F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080792	NM_001372108.2(DDO):c.221A>G (p.His74Arg)	DDO (H20R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2545883	NM_001372108.2(DDO):c.218A>G (p.Asn73Ser)	DDO (N19S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2213018	NM_001372108.2(DDO):c.136G>A (p.Val46Met)	DDO (V46M)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3080791	NM_001372108.2(DDO):c.83G>A (p.Arg28Gln)	DDO (R28Q)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GLikely benign
Select item 3271215	NM_001372108.2(DDO):c.62G>A (p.Cys21Tyr)	DDO (C21Y)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2388725	NM_001372108.2(DDO):c.13C>T (p.Arg5Trp)	DDO (R5W)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3080802	NM_001372108.2(DDO):c.7A>G (p.Thr3Ala)	DDO (T3A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3080799	NM_001372108.2(DDO):c.-11G>A	DDO	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2490328	NM_001372108.2(DDO):c.-20G>C	DDO	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2594472	NM_001372108.2(DDO):c.-36G>C	DDO	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3080790	NM_001372108.2(DDO):c.-71G>A	DDO	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 33