DDX52[gene] and "single gene"[properties] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2317041	NM_007010.5(DDX52):c.1737T>A (p.Asp579Glu)	DDX52 (D471E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384246	NM_007010.5(DDX52):c.1645C>G (p.Leu549Val)	DDX52 (L441V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081112	NM_007010.5(DDX52):c.1591A>T (p.Ile531Leu)	DDX52 (I423L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380422	NM_007010.5(DDX52):c.1579G>A (p.Val527Ile)	DDX52 (V527I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081111	NM_007010.5(DDX52):c.1392G>C (p.Trp464Cys)	DDX52 (W356C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530520	NM_007010.5(DDX52):c.1356T>G (p.Asp452Glu)	DDX52 (D452E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 993894	NM_007010.5(DDX52):c.1301_1302del (p.Ile433_Tyr434insTer)	DDX52	Microsatellite (nonsense)	not provided	GUncertain significance
Select item 3081110	NM_007010.5(DDX52):c.1109A>G (p.Asn370Ser)	DDX52 (N262S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558434	NM_007010.5(DDX52):c.1076A>T (p.Asp359Val)	DDX52 (D251V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282724	NM_007010.5(DDX52):c.1061C>T (p.Ala354Val)	DDX52 (A246V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553285	NM_007010.5(DDX52):c.1031C>T (p.Ser344Phe)	DDX52 (S236F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081109	NM_007010.5(DDX52):c.1006G>C (p.Ala336Pro)	DDX52 (A228P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271361	NM_007010.5(DDX52):c.977A>G (p.Asp326Gly)	DDX52 (D218G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081116	NM_007010.5(DDX52):c.882T>A (p.Asn294Lys)	DDX52 (N294K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348530	NM_007010.5(DDX52):c.877C>A (p.Pro293Thr)	DDX52 (P293T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336709	NM_007010.5(DDX52):c.862A>C (p.Ile288Leu)	DDX52 (I288L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081115	NM_007010.5(DDX52):c.833T>C (p.Phe278Ser)	DDX52 (F278S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310532	NM_007010.5(DDX52):c.797A>G (p.His266Arg)	DDX52 (H158R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219044	NM_007010.5(DDX52):c.782C>T (p.Thr261Ile)	DDX52 (T261I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236617	NM_007010.5(DDX52):c.739G>A (p.Ala247Thr)	DDX52 (A139T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255941	NM_007010.5(DDX52):c.721T>C (p.Ser241Pro)	DDX52 (S133P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081114	NM_007010.5(DDX52):c.662T>G (p.Ile221Ser)	DDX52 (I113S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081113	NM_007010.5(DDX52):c.566C>T (p.Thr189Met)	DDX52 (T81M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319999	NM_007010.5(DDX52):c.448C>T (p.His150Tyr)	DDX52 (H150Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342976	NM_007010.5(DDX52):c.431G>A (p.Arg144Gln)	DDX52 (R36Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209669	NM_007010.5(DDX52):c.407G>C (p.Arg136Thr)	DDX52 (R28T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540906	NM_007010.5(DDX52):c.388G>A (p.Gly130Arg)	DDX52 (G22R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354692	NM_007010.5(DDX52):c.361G>C (p.Val121Leu)	DDX52 (V121L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281943	NM_007010.5(DDX52):c.187C>G (p.Gln63Glu)	DDX52 (Q63E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 29