DXO[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086409	NM_005510.4(DXO):c.1139A>C (p.Glu380Ala)	DXO (E380A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317880	NM_005510.4(DXO):c.1081G>C (p.Val361Leu)	DXO (V291L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259059	NM_005510.4(DXO):c.1045C>T (p.Leu349Phe)	DXO (L165F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274128	NM_005510.4(DXO):c.1022C>T (p.Thr341Met)	DXO (T157M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507589	NM_005510.4(DXO):c.956G>A (p.Arg319His)	DXO (R135H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463995	NM_005510.4(DXO):c.902C>T (p.Ser301Phe)	DXO (S117F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371526	NM_005510.4(DXO):c.767C>T (p.Thr256Ile)	DXO (T256I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407125	NM_005510.4(DXO):c.661C>T (p.Arg221Cys)	DXO (R37C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086413	NM_005510.4(DXO):c.554T>C (p.Met185Thr)	DXO (M1T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086412	NM_005510.4(DXO):c.530G>A (p.Arg177Gln)	DXO (R177Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2343026	NM_005510.4(DXO):c.529C>T (p.Arg177Trp)	DXO (R177W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2543547	NM_005510.4(DXO):c.503C>T (p.Pro168Leu)	DXO (P168L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3086411	NM_005510.4(DXO):c.500C>T (p.Thr167Ile)	DXO (T167I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2466660	NM_005510.4(DXO):c.450G>C (p.Gln150His)	DXO (Q150H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2622804	NM_005510.4(DXO):c.434G>A (p.Arg145Gln)	DXO (R145Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3274129	NM_005510.4(DXO):c.402C>A (p.His134Gln)	DXO (H134Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance