DNASE2[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1063143	NM_001375.3(DNASE2):c.1079T>G (p.Ile360Ser)	DNASE2 (I360S)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2009154	NM_001375.3(DNASE2):c.1060C>G (p.Pro354Ala)	DNASE2 (P354A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2324924	NM_001375.3(DNASE2):c.1050G>A (p.Met350Ile)	DNASE2 (M350I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1935743	NM_001375.3(DNASE2):c.1040G>A (p.Cys347Tyr)	DNASE2 (C347Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1498679	NM_001375.3(DNASE2):c.1021G>T (p.Val341Leu)	DNASE2 (V341L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1946418	NM_001375.3(DNASE2):c.1020G>A (p.Leu340=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1585475	NM_001375.3(DNASE2):c.1017G>A (p.Pro339=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2119898	NM_001375.3(DNASE2):c.1016C>A (p.Pro339Gln)	DNASE2 (P339Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1346441	NM_001375.3(DNASE2):c.1016C>T (p.Pro339Leu)	DNASE2 (P339L)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1974914	NM_001375.3(DNASE2):c.1008C>T (p.Ala336=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2060400	NM_001375.3(DNASE2):c.996C>T (p.Ala332=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1493258	NM_001375.3(DNASE2):c.995C>A (p.Ala332Asp)	DNASE2 (A332D)	Single nucleotide variant (missense variant)	Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency +1 more	GUncertain significance
Select item 810670	NM_001375.3(DNASE2):c.965G>A (p.Gly322Asp)	DNASE2 (G322D)	Single nucleotide variant (missense variant)	Systemic lupus erythematosus	GUncertain significance
Select item 1395765	NM_001375.3(DNASE2):c.962G>A (p.Arg321Gln)	DNASE2 (R321Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2158525	NM_001375.3(DNASE2):c.961C>T (p.Arg321Trp)	DNASE2 (R321W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2963393	NM_001375.3(DNASE2):c.945C>T (p.Asn315=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1348580	NM_001375.3(DNASE2):c.941G>A (p.Arg314Gln)	DNASE2 (R314Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1523415	NM_001375.3(DNASE2):c.940C>T (p.Arg314Trp)	DNASE2 (R314W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1491986	NM_001375.3(DNASE2):c.925G>T (p.Val309Leu)	DNASE2 (V309L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1349577	NM_001375.3(DNASE2):c.925G>A (p.Val309Met)	DNASE2 (V309M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2780636	NM_001375.3(DNASE2):c.912G>T (p.Gly304=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2092797	NM_001375.3(DNASE2):c.911G>A (p.Gly304Glu)	DNASE2 (G304E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1469268	NM_001375.3(DNASE2):c.905C>T (p.Pro302Leu)	DNASE2 (P302L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1615138	NM_001375.3(DNASE2):c.900G>A (p.Val300=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2138240	NM_001375.3(DNASE2):c.898G>A (p.Val300Met)	DNASE2 (V300M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1672006	NM_001375.3(DNASE2):c.897C>T (p.Cys299=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2539687	NM_001375.3(DNASE2):c.893G>T (p.Trp298Leu)	DNASE2 (W298L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2695668	NM_001375.3(DNASE2):c.879G>A (p.Glu293=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2107495	NM_001375.3(DNASE2):c.876A>G (p.Thr292=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1559102	NM_001375.3(DNASE2):c.873C>T (p.Ser291=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1492191	NM_001375.3(DNASE2):c.856G>A (p.Gly286Ser)	DNASE2 (G286S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1164634	NM_001375.3(DNASE2):c.843C>T (p.Phe281=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1002449	NM_001375.3(DNASE2):c.837A>G (p.Ile279Met)	DNASE2 (I279M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2489869	NM_001375.3(DNASE2):c.830A>G (p.Asn277Ser)	DNASE2 (N277S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2067417	NM_001375.3(DNASE2):c.821T>G (p.Leu274Arg)	DNASE2 (L274R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1518603	NM_001375.3(DNASE2):c.812G>A (p.Trp271Ter)	DNASE2 (W271*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2070794	NM_001375.3(DNASE2):c.808A>G (p.Ile270Val)	DNASE2 (I270V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1443189	NM_001375.3(DNASE2):c.804G>A (p.Ser268=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3084630	NM_001375.3(DNASE2):c.800G>C (p.Cys267Ser)	DNASE2 (C267S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1926522	NM_001375.3(DNASE2):c.777T>C (p.Thr259=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1573450	NM_001375.3(DNASE2):c.774A>G (p.Lys258=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2328704	NM_001375.3(DNASE2):c.740T>G (p.Leu247Arg)	DNASE2 (L247R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1510924	NM_001375.3(DNASE2):c.721G>A (p.Gly241Ser)	DNASE2 (G241S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2959409	NM_001375.3(DNASE2):c.720C>T (p.Ser240=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1547726	NM_001375.3(DNASE2):c.710-19C>T	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2842337	NM_001375.3(DNASE2):c.709+20G>C	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1653807	NM_001375.3(DNASE2):c.709+19G>T	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1968532	NM_001375.3(DNASE2):c.709+9C>T	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1510198	NM_001375.3(DNASE2):c.709+4A>T	DNASE2	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance
Select item 1511111	NM_001375.3(DNASE2):c.685_686delinsCT (p.Ala229Leu)	DNASE2 (A229L)	Indel (missense variant)	not provided	GUncertain significance
Select item 2052625	NM_001375.3(DNASE2):c.664G>A (p.Gly222Arg)	DNASE2 (G222R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1531053	NM_001375.3(DNASE2):c.663C>T (p.Ala221=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1915164	NM_001375.3(DNASE2):c.653C>T (p.Thr218Ile)	DNASE2 (T218I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1350621	NM_001375.3(DNASE2):c.647C>T (p.Thr216Ile)	DNASE2 (T216I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1503676	NM_001375.3(DNASE2):c.636C>A (p.Asn212Lys)	DNASE2 (N212K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1917118	NM_001375.3(DNASE2):c.630C>T (p.Pro210=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1509079	NM_001375.3(DNASE2):c.626A>G (p.Glu209Gly)	DNASE2 (E209G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2077853	NM_001375.3(DNASE2):c.625G>T (p.Glu209Ter)	DNASE2 (E209*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1395526	NM_001375.3(DNASE2):c.621C>G (p.Ser207Arg)	DNASE2 (S207R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1539755	NM_001375.3(DNASE2):c.616G>A (p.Val206Ile)	DNASE2 (V206I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3000553	NM_001375.3(DNASE2):c.615C>T (p.His205=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1164325	NM_001375.3(DNASE2):c.611A>G (p.His204Arg)	DNASE2 (H204R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1916061	NM_001375.3(DNASE2):c.601G>A (p.Val201Ile)	DNASE2 (V201I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2417725	NM_001375.3(DNASE2):c.585C>T (p.Pro195=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2138241	NM_001375.3(DNASE2):c.575A>C (p.Gln192Pro)	DNASE2 (Q192P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1985157	NM_001375.3(DNASE2):c.565A>T (p.Ile189Phe)	DNASE2 (I189F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2090432	NM_001375.3(DNASE2):c.552C>G (p.Tyr184Ter)	DNASE2 (Y184*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2110478	NM_001375.3(DNASE2):c.542T>C (p.Val181Ala)	DNASE2 (V181A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2037004	NM_001375.3(DNASE2):c.533A>G (p.Tyr178Cys)	DNASE2 (Y178C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2893182	NM_001375.3(DNASE2):c.512-6del	DNASE2	Deletion (intron variant)	not provided	GLikely benign
Select item 2707369	NM_001375.3(DNASE2):c.512-11T>G	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1576897	NM_001375.3(DNASE2):c.512-12C>T	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1908809	NM_001375.3(DNASE2):c.512-15C>T	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993868	NM_001375.3(DNASE2):c.511+16G>A	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2699026	NM_001375.3(DNASE2):c.511+15G>A	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1577529	NM_001375.3(DNASE2):c.511+8G>A	DNASE2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1463731	NM_001375.3(DNASE2):c.511+5G>A	DNASE2	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1374279	NM_001375.3(DNASE2):c.510G>A (p.Met170Ile)	DNASE2 (M170I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2058616	NM_001375.3(DNASE2):c.509T>C (p.Met170Thr)	DNASE2 (M170T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1673650	NM_001375.3(DNASE2):c.504G>A (p.Ser168=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1494006	NM_001375.3(DNASE2):c.503C>G (p.Ser168Trp)	DNASE2 (S168W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1367521	NM_001375.3(DNASE2):c.503C>T (p.Ser168Leu)	DNASE2 (S168L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1988172	NM_001375.3(DNASE2):c.493G>A (p.Ala165Thr)	DNASE2 (A165T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2986567	NM_001375.3(DNASE2):c.492C>T (p.Phe164=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1525461	NM_001375.3(DNASE2):c.487C>T (p.Pro163Ser)	DNASE2 (P163S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1351974	NM_001375.3(DNASE2):c.477T>G (p.Cys159Trp)	DNASE2 (C159W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2637371	NM_001375.3(DNASE2):c.463C>G (p.Gln155Glu)	DNASE2 (Q155E)	Single nucleotide variant (missense variant)	DNASE2-related disorder	GUncertain significance
Select item 1569427	NM_001375.3(DNASE2):c.459C>T (p.Tyr153=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2177697	NM_001375.3(DNASE2):c.450C>T (p.Ala150=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1907083	NM_001375.3(DNASE2):c.448G>A (p.Ala150Thr)	DNASE2 (A150T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2091872	NM_001375.3(DNASE2):c.434_435delinsTT (p.Ser145Ile)	DNASE2 (S145I)	Indel (missense variant)	not provided	GUncertain significance
Select item 1168081	NM_001375.3(DNASE2):c.435C>T (p.Ser145=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1467114	NM_001375.3(DNASE2):c.425C>T (p.Ala142Val)	DNASE2 (A142V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2000500	NM_001375.3(DNASE2):c.421T>C (p.Ser141Pro)	DNASE2 (S141P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2718725	NM_001375.3(DNASE2):c.417C>A (p.Ala139=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1372419	NM_001375.3(DNASE2):c.414G>A (p.Pro138=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1417856	NM_001375.3(DNASE2):c.413C>T (p.Pro138Leu)	DNASE2 (P138L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1461878	NM_001375.3(DNASE2):c.403T>C (p.Phe135Leu)	DNASE2 (F135L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1957763	NM_001375.3(DNASE2):c.400A>C (p.Asn134His)	DNASE2 (N134H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2870525	NM_001375.3(DNASE2):c.393T>C (p.Ser131=)	DNASE2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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