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

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2272658	NM_016286.4(DCXR):c.724T>G (p.Trp242Gly)	DCXR (W242G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315052	NM_016286.4(DCXR):c.706C>G (p.Pro236Ala)	DCXR (P236A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080691	NM_016286.4(DCXR):c.688A>T (p.Thr230Ser)	DCXR (T228S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271175	NM_016286.4(DCXR):c.587A>C (p.Lys196Thr)	DCXR (K196T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080690	NM_016286.4(DCXR):c.584A>G (p.His195Arg)	DCXR (H195R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247054	NM_016286.4(DCXR):c.478A>G (p.Thr160Ala)	DCXR (T160A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080689	NM_016286.4(DCXR):c.463G>T (p.Ala155Ser)	DCXR (A153S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589424	NM_016286.4(DCXR):c.360G>C (p.Arg120Ser)	DCXR (R120S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597878	NM_016286.4(DCXR):c.358A>G (p.Arg120Gly)	DCXR (R118G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590974	NM_016286.4(DCXR):c.321C>A (p.Asn107Lys)	DCXR (N105K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299970	NM_016286.4(DCXR):c.315G>C (p.Glu105Asp)	DCXR (E105D +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3080687	NM_016286.4(DCXR):c.260C>T (p.Ala87Val)	DCXR (A87V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510902	NM_016286.4(DCXR):c.145C>T (p.Arg49Cys)	DCXR, LOC130061998 (R47C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358906	NM_016286.4(DCXR):c.118A>G (p.Thr40Ala)	DCXR, LOC130061998 (T38A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356889	NM_016286.4(DCXR):c.118A>C (p.Thr40Pro)	DCXR, LOC130061998 (T38P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393048	NM_016286.4(DCXR):c.114C>G (p.Ser38Arg)	DCXR, LOC130061998 (S38R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080692	NM_016286.4(DCXR):c.89C>T (p.Thr30Met)	DCXR, LOC130061998 (T28M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225730	NM_016286.4(DCXR):c.26G>T (p.Arg9Leu)	DCXR, LOC130061998 (R9L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080686	NM_016286.4(DCXR):c.17C>T (p.Ala6Val)	DCXR, LOC130061998 (A6V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343078	NM_016286.4(DCXR):c.10T>C (p.Phe4Leu)	DCXR, LOC130061998 (F4L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 20