ZNF516[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2604705	NM_014643.4(ZNF516):c.3214C>A (p.Leu1072Ile)	ZNF516 (L1072I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291098	NM_014643.4(ZNF516):c.3104C>T (p.Ala1035Val)	ZNF516 (A1035V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253396	NM_014643.4(ZNF516):c.3094G>A (p.Val1032Met)	ZNF516 (V1032M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258486	NM_014643.4(ZNF516):c.3070G>A (p.Ala1024Thr)	ZNF516 (A1024T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2648815	NM_014643.4(ZNF516):c.3066C>T (p.Gly1022=)	ZNF516	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2387299	NM_014643.4(ZNF516):c.3056G>T (p.Gly1019Val)	ZNF516 (G1019V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196363	NM_014643.4(ZNF516):c.3029T>C (p.Leu1010Pro)	ZNF516 (L1010P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221028	NM_014643.4(ZNF516):c.3022C>A (p.Gln1008Lys)	ZNF516 (Q1008K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196361	NM_014643.4(ZNF516):c.2999G>A (p.Arg1000His)	ZNF516 (R1000H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570002	NM_014643.4(ZNF516):c.2980G>A (p.Ala994Thr)	ZNF516 (A994T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2648816	NM_014643.4(ZNF516):c.2913G>A (p.Pro971=)	ZNF516	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3196358	NM_014643.4(ZNF516):c.2894C>G (p.Thr965Arg)	ZNF516 (T965R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258485	NM_014643.4(ZNF516):c.2873C>T (p.Ala958Val)	ZNF516 (A958V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3196357	NM_014643.4(ZNF516):c.2846C>T (p.Pro949Leu)	ZNF516 (P949L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258493	NM_014643.4(ZNF516):c.2831C>T (p.Ser944Leu)	ZNF516 (S944L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196356	NM_014643.4(ZNF516):c.2824C>G (p.Gln942Glu)	ZNF516 (Q942E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354083	NM_014643.4(ZNF516):c.2795C>T (p.Thr932Met)	ZNF516 (T932M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467944	NM_014643.4(ZNF516):c.2762G>A (p.Gly921Asp)	ZNF516 (G921D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408074	NM_014643.4(ZNF516):c.2745A>C (p.Lys915Asn)	ZNF516 (K915N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408073	NM_014643.4(ZNF516):c.2720A>C (p.Lys907Thr)	ZNF516 (K907T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346987	NM_014643.4(ZNF516):c.2706G>C (p.Gln902His)	ZNF516 (Q902H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273220	NM_014643.4(ZNF516):c.2699C>T (p.Ala900Val)	ZNF516 (A900V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258483	NM_014643.4(ZNF516):c.2661G>C (p.Gln887His)	ZNF516 (Q887H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722417	NM_014643.4(ZNF516):c.2626G>T (p.Ala876Ser)	ZNF516 (A876S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2292349	NM_014643.4(ZNF516):c.2623T>C (p.Cys875Arg)	ZNF516 (C875R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196355	NM_014643.4(ZNF516):c.2607C>A (p.Ser869Arg)	ZNF516 (S869R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196354	NM_014643.4(ZNF516):c.2603A>G (p.Glu868Gly)	ZNF516 (E868G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196353	NM_014643.4(ZNF516):c.2581G>A (p.Ala861Thr)	ZNF516 (A861T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527001	NM_014643.4(ZNF516):c.2510G>A (p.Arg837His)	ZNF516 (R837H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196352	NM_014643.4(ZNF516):c.2414G>A (p.Ser805Asn)	ZNF516 (S805N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3258484	NM_014643.4(ZNF516):c.2410A>G (p.Arg804Gly)	ZNF516 (R804G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514096	NM_014643.4(ZNF516):c.2396G>A (p.Gly799Asp)	ZNF516 (G799D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196351	NM_014643.4(ZNF516):c.2393A>G (p.Asn798Ser)	ZNF516 (N798S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376558	NM_014643.4(ZNF516):c.2363A>G (p.Asn788Ser)	ZNF516 (N788S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2623010	NM_014643.4(ZNF516):c.2360G>A (p.Cys787Tyr)	ZNF516 (C787Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471099	NM_014643.4(ZNF516):c.2338C>T (p.Arg780Cys)	ZNF516 (R780C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196350	NM_014643.4(ZNF516):c.2302A>G (p.Lys768Glu)	ZNF516 (K768E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214736	NM_014643.4(ZNF516):c.2264C>T (p.Ala755Val)	ZNF516 (A755V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539409	NM_014643.4(ZNF516):c.2252C>T (p.Ser751Phe)	ZNF516 (S751F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214935	NM_014643.4(ZNF516):c.2242G>A (p.Glu748Lys)	ZNF516 (E748K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352908	NM_014643.4(ZNF516):c.2236A>G (p.Asn746Asp)	ZNF516 (N746D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488229	NM_014643.4(ZNF516):c.2213G>A (p.Arg738Lys)	ZNF516 (R738K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612085	NM_014643.4(ZNF516):c.2192T>C (p.Met731Thr)	ZNF516 (M731T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405523	NM_014643.4(ZNF516):c.2188C>T (p.Leu730Phe)	ZNF516 (L730F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333829	NM_014643.4(ZNF516):c.2173G>A (p.Ala725Thr)	ZNF516 (A725T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196349	NM_014643.4(ZNF516):c.2156C>G (p.Ser719Cys)	ZNF516 (S719C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490115	NM_014643.4(ZNF516):c.2156C>T (p.Ser719Phe)	ZNF516 (S719F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608638	NM_014643.4(ZNF516):c.2152C>T (p.His718Tyr)	ZNF516 (H718Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205255	NM_014643.4(ZNF516):c.2127G>T (p.Lys709Asn)	ZNF516 (K709N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196348	NM_014643.4(ZNF516):c.2108C>T (p.Thr703Met)	ZNF516 (T703M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2205505	NM_014643.4(ZNF516):c.2090C>T (p.Thr697Met)	ZNF516 (T697M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196347	NM_014643.4(ZNF516):c.2056G>C (p.Val686Leu)	ZNF516 (V686L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356040	NM_014643.4(ZNF516):c.2056G>A (p.Val686Ile)	ZNF516 (V686I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526640	NM_014643.4(ZNF516):c.1946C>G (p.Ser649Cys)	ZNF516 (S649C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400597	NM_014643.4(ZNF516):c.1918G>A (p.Gly640Ser)	ZNF516 (G640S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3196346	NM_014643.4(ZNF516):c.1900G>A (p.Ala634Thr)	ZNF516 (A634T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290208	NM_014643.4(ZNF516):c.1900G>T (p.Ala634Ser)	ZNF516 (A634S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457896	NM_014643.4(ZNF516):c.1867A>G (p.Ser623Gly)	ZNF516 (S623G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196345	NM_014643.4(ZNF516):c.1826G>A (p.Arg609His)	ZNF516 (R609H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2510791	NM_014643.4(ZNF516):c.1823G>A (p.Arg608His)	ZNF516 (R608H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2545246	NM_014643.4(ZNF516):c.1822C>T (p.Arg608Cys)	ZNF516 (R608C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509344	NM_014643.4(ZNF516):c.1820C>T (p.Pro607Leu)	ZNF516 (P607L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258494	NM_014643.4(ZNF516):c.1771G>A (p.Glu591Lys)	ZNF516 (E591K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790745	NM_014643.4(ZNF516):c.1753C>T (p.Leu585=)	ZNF516	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3196344	NM_014643.4(ZNF516):c.1724G>A (p.Cys575Tyr)	ZNF516 (C575Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539493	NM_014643.4(ZNF516):c.1720G>A (p.Ala574Thr)	ZNF516 (A574T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613356	NM_014643.4(ZNF516):c.1696T>A (p.Ser566Thr)	ZNF516 (S566T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459945	NM_014643.4(ZNF516):c.1691C>G (p.Ser564Trp)	ZNF516 (S564W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196343	NM_014643.4(ZNF516):c.1678A>C (p.Ser560Arg)	ZNF516 (S560R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208425	NM_014643.4(ZNF516):c.1663C>T (p.Arg555Cys)	ZNF516 (R555C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196342	NM_014643.4(ZNF516):c.1658G>A (p.Arg553Gln)	ZNF516 (R553Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259113	NM_014643.4(ZNF516):c.1645G>A (p.Asp549Asn)	ZNF516 (D549N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258491	NM_014643.4(ZNF516):c.1642G>A (p.Gly548Arg)	ZNF516 (G548R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455235	NM_014643.4(ZNF516):c.1583A>G (p.His528Arg)	ZNF516 (H528R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474001	NM_014643.4(ZNF516):c.1510A>G (p.Arg504Gly)	ZNF516 (R504G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615777	NM_014643.4(ZNF516):c.1502C>A (p.Pro501His)	ZNF516 (P501H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280693	NM_014643.4(ZNF516):c.1480G>C (p.Asp494His)	ZNF516 (D494H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196341	NM_014643.4(ZNF516):c.1463C>T (p.Ala488Val)	ZNF516 (A488V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333528	NM_014643.4(ZNF516):c.1418C>T (p.Ala473Val)	ZNF516 (A473V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196340	NM_014643.4(ZNF516):c.1417G>A (p.Ala473Thr)	ZNF516 (A473T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258488	NM_014643.4(ZNF516):c.1379G>A (p.Ser460Asn)	ZNF516 (S460N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383540	NM_014643.4(ZNF516):c.1360C>T (p.Arg454Cys)	ZNF516 (R454C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489851	NM_014643.4(ZNF516):c.1268C>T (p.Thr423Met)	ZNF516 (T423M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258487	NM_014643.4(ZNF516):c.1202C>T (p.Thr401Met)	ZNF516 (T401M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196339	NM_014643.4(ZNF516):c.1172C>T (p.Pro391Leu)	ZNF516 (P391L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487494	NM_014643.4(ZNF516):c.1096C>A (p.Arg366Ser)	ZNF516 (R366S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491861	NM_014643.4(ZNF516):c.1064C>A (p.Ala355Asp)	ZNF516 (A355D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298811	NM_014643.4(ZNF516):c.1054G>A (p.Ala352Thr)	ZNF516 (A352T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221026	NM_014643.4(ZNF516):c.941C>T (p.Pro314Leu)	ZNF516 (P314L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232165	NM_014643.4(ZNF516):c.922C>A (p.Pro308Thr)	ZNF516 (P308T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266127	NM_014643.4(ZNF516):c.905C>T (p.Thr302Met)	ZNF516 (T302M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790746	NM_014643.4(ZNF516):c.870C>T (p.Phe290=)	ZNF516	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2275109	NM_014643.4(ZNF516):c.783G>C (p.Trp261Cys)	ZNF516 (W261C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534929	NM_014643.4(ZNF516):c.688G>A (p.Gly230Ser)	ZNF516 (G230S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455312	NM_014643.4(ZNF516):c.683G>A (p.Gly228Glu)	ZNF516 (G228E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196371	NM_014643.4(ZNF516):c.680A>G (p.Gln227Arg)	ZNF516 (Q227R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258489	NM_014643.4(ZNF516):c.623C>T (p.Ala208Val)	ZNF516 (A208V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2231270	NM_014643.4(ZNF516):c.620A>T (p.Tyr207Phe)	ZNF516 (Y207F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214018	NM_014643.4(ZNF516):c.587C>T (p.Ala196Val)	ZNF516 (A196V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196369	NM_014643.4(ZNF516):c.581A>G (p.His194Arg)	ZNF516 (H194R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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