"Ambry Genetics"[submitter] AND "LOC130061998"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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

ClinVar