ClinVar for Gene (Select 24149) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3195116	NM_014345.3(ZNF318):c.947G>A (p.Arg316Gln)	ZNF318 (R316Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195115	NM_014345.3(ZNF318):c.893A>G (p.Asn298Ser)	ZNF318 (N298S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195114	NM_014345.3(ZNF318):c.853A>G (p.Met285Val)	ZNF318 (M285V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195113	NM_014345.3(ZNF318):c.709A>G (p.Ser237Gly)	ZNF318 (S237G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195112	NM_014345.3(ZNF318):c.659T>A (p.Leu220His)	ZNF318 (L220H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195111	NM_014345.3(ZNF318):c.6451C>G (p.Leu2151Val)	ZNF318 (L2151V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195110	NM_014345.3(ZNF318):c.6145G>A (p.Val2049Ile)	ZNF318 (V2049I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195109	NM_014345.3(ZNF318):c.6136G>A (p.Glu2046Lys)	ZNF318 (E2046K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195108	NM_014345.3(ZNF318):c.5710T>G (p.Leu1904Val)	ZNF318 (L1904V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195107	NM_014345.3(ZNF318):c.5648C>G (p.Thr1883Arg)	ZNF318 (T1883R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195106	NM_014345.3(ZNF318):c.5313A>C (p.Arg1771Ser)	ZNF318 (R1771S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195105	NM_014345.3(ZNF318):c.5251C>T (p.Leu1751Phe)	ZNF318 (L1751F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195103	NM_014345.3(ZNF318):c.494G>A (p.Arg165Gln)	ZNF318 (R165Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195102	NM_014345.3(ZNF318):c.4823A>G (p.Lys1608Arg)	ZNF318 (K1608R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195101	NM_014345.3(ZNF318):c.4481A>G (p.Asn1494Ser)	ZNF318 (N1494S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195100	NM_014345.3(ZNF318):c.4303C>T (p.His1435Tyr)	ZNF318 (H1435Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195099	NM_014345.3(ZNF318):c.4153A>G (p.Thr1385Ala)	ZNF318 (T1385A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195098	NM_014345.3(ZNF318):c.3947A>C (p.Lys1316Thr)	ZNF318 (K1316T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195097	NM_014345.3(ZNF318):c.3899T>A (p.Ile1300Asn)	ZNF318 (I1300N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195096	NM_014345.3(ZNF318):c.3706C>G (p.Gln1236Glu)	ZNF318 (Q1236E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195095	NM_014345.3(ZNF318):c.3648G>C (p.Lys1216Asn)	ZNF318 (K1216N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195094	NM_014345.3(ZNF318):c.3545G>A (p.Arg1182His)	ZNF318 (R1182H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195093	NM_014345.3(ZNF318):c.3159G>T (p.Gln1053His)	ZNF318 (Q1053H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195092	NM_014345.3(ZNF318):c.3116A>G (p.Lys1039Arg)	ZNF318 (K1039R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195090	NM_014345.3(ZNF318):c.2677G>A (p.Glu893Lys)	ZNF318 (E893K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195089	NM_014345.3(ZNF318):c.2576C>T (p.Ala859Val)	ZNF318 (A859V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195088	NM_014345.3(ZNF318):c.2470A>G (p.Ile824Val)	ZNF318 (I824V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3195086	NM_014345.3(ZNF318):c.2359T>A (p.Ser787Thr)	ZNF318 (S787T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195085	NM_014345.3(ZNF318):c.2258C>A (p.Pro753Gln)	ZNF318 (P753Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195084	NM_014345.3(ZNF318):c.2236C>T (p.Pro746Ser)	ZNF318 (P746S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195083	NM_014345.3(ZNF318):c.2189G>C (p.Ser730Thr)	ZNF318 (S730T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195082	NM_014345.3(ZNF318):c.208C>T (p.Pro70Ser)	LOC129996504, ZNF318 (P70S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195081	NM_014345.3(ZNF318):c.2059C>T (p.His687Tyr)	ZNF318 (H687Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195080	NM_014345.3(ZNF318):c.1967G>A (p.Arg656His)	ZNF318 (R656H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195079	NM_014345.3(ZNF318):c.158C>T (p.Pro53Leu)	LOC129996504, ZNF318 (P53L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195077	NM_014345.3(ZNF318):c.1496G>A (p.Arg499Lys)	ZNF318 (R499K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195076	NM_014345.3(ZNF318):c.1410T>G (p.Phe470Leu)	ZNF318 (F470L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195075	NM_014345.3(ZNF318):c.133C>G (p.Pro45Ala)	LOC129996504, ZNF318 (P45A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195074	NM_014345.3(ZNF318):c.1238A>C (p.Tyr413Ser)	ZNF318 (Y413S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656597	NM_014345.3(ZNF318):c.1920T>C (p.Phe640=)	ZNF318	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656596	NM_014345.3(ZNF318):c.5058T>C (p.Tyr1686=)	ZNF318	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656595	NM_014345.3(ZNF318):c.5904C>G (p.Thr1968=)	ZNF318	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656594	NM_014345.3(ZNF318):c.6171C>T (p.Ser2057=)	ZNF318	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2621838	NM_014345.3(ZNF318):c.6721T>G (p.Ser2241Ala)	ZNF318 (S2241A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620577	NM_014345.3(ZNF318):c.2084A>G (p.His695Arg)	ZNF318 (H695R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612353	NM_014345.3(ZNF318):c.6790A>G (p.Thr2264Ala)	ZNF318 (T2264A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2608460	NM_014345.3(ZNF318):c.5306A>T (p.Asp1769Val)	ZNF318 (D1769V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606837	NM_014345.3(ZNF318):c.5807G>C (p.Arg1936Thr)	ZNF318 (R1936T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601989	NM_014345.3(ZNF318):c.2474C>G (p.Thr825Ser)	ZNF318 (T825S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600799	NM_014345.3(ZNF318):c.2723A>T (p.Lys908Met)	ZNF318 (K908M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599050	NM_014345.3(ZNF318):c.4471G>A (p.Val1491Met)	ZNF318 (V1491M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597698	NM_014345.3(ZNF318):c.4414A>G (p.Ile1472Val)	ZNF318 (I1472V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2590981	NM_014345.3(ZNF318):c.931C>T (p.Leu311Phe)	ZNF318 (L311F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559512	NM_014345.3(ZNF318):c.6764T>C (p.Val2255Ala)	ZNF318 (V2255A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557747	NM_014345.3(ZNF318):c.6178G>A (p.Ala2060Thr)	ZNF318 (A2060T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2555716	NM_014345.3(ZNF318):c.4988G>A (p.Gly1663Asp)	ZNF318 (G1663D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2540456	NM_014345.3(ZNF318):c.4835C>T (p.Thr1612Ile)	ZNF318 (T1612I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537258	NM_014345.3(ZNF318):c.17C>G (p.Ala6Gly)	ZNF318 (A6G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529584	NM_014345.3(ZNF318):c.3382G>C (p.Glu1128Gln)	ZNF318 (E1128Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517539	NM_014345.3(ZNF318):c.6082C>T (p.Arg2028Trp)	ZNF318 (R2028W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513014	NM_014345.3(ZNF318):c.130C>G (p.Pro44Ala)	LOC129996504, ZNF318 (P44A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512948	NM_014345.3(ZNF318):c.508C>T (p.Arg170Trp)	ZNF318 (R170W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511331	NM_014345.3(ZNF318):c.5704A>G (p.Met1902Val)	ZNF318 (M1902V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2507877	NM_014345.3(ZNF318):c.6674T>G (p.Val2225Gly)	ZNF318 (V2225G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493438	NM_014345.3(ZNF318):c.2407C>T (p.Pro803Ser)	ZNF318 (P803S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492473	NM_014345.3(ZNF318):c.3641A>G (p.Glu1214Gly)	ZNF318 (E1214G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489562	NM_014345.3(ZNF318):c.2646G>T (p.Lys882Asn)	ZNF318 (K882N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489519	NM_014345.3(ZNF318):c.2632A>G (p.Ile878Val)	ZNF318 (I878V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476313	NM_014345.3(ZNF318):c.1824T>G (p.Ile608Met)	ZNF318 (I608M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471196	NM_014345.3(ZNF318):c.1231C>A (p.Pro411Thr)	ZNF318 (P411T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459906	NM_014345.3(ZNF318):c.277C>T (p.Pro93Ser)	LOC129996503, ZNF318 (P93S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457122	NM_014345.3(ZNF318):c.6190C>A (p.Pro2064Thr)	ZNF318 (P2064T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456368	NM_014345.3(ZNF318):c.6713C>A (p.Ala2238Asp)	ZNF318 (A2238D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2424354	NC_000006.11:g.(?_42162409)_(44154249_?)del	KLC4, POLR1C +43 more	Deletion	not provided	GUncertain significance
Select item 2422887	NC_000006.11:g.(?_41126341)_(43737486_?)dup	ABCC10, BICRAL +57 more	Duplication	PRPH2-related disorder	GUncertain significance
Select item 2422814	NC_000006.11:g.(?_41126341)_(43752536_?)del	ABCC10, BICRAL +58 more	Deletion	Peroxisome biogenesis disorder	GPathogenic
Select item 2408575	NM_014345.3(ZNF318):c.1898G>A (p.Arg633His)	ZNF318 (R633H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403727	NM_014345.3(ZNF318):c.1795A>G (p.Ile599Val)	ZNF318 (I599V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399797	NM_014345.3(ZNF318):c.6802G>A (p.Ala2268Thr)	ZNF318 (A2268T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399755	NM_014345.3(ZNF318):c.698G>A (p.Arg233Gln)	ZNF318 (R233Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394229	NM_014345.3(ZNF318):c.385G>A (p.Asp129Asn)	ZNF318 (D129N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393691	NM_014345.3(ZNF318):c.3068A>G (p.Asn1023Ser)	ZNF318 (N1023S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387100	NM_014345.3(ZNF318):c.2280G>T (p.Gln760His)	ZNF318 (Q760H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382178	NM_014345.3(ZNF318):c.152G>A (p.Arg51Gln)	LOC129996504, ZNF318 (R51Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375828	NM_014345.3(ZNF318):c.6824C>G (p.Ser2275Cys)	ZNF318 (S2275C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375827	NM_014345.3(ZNF318):c.5824A>G (p.Arg1942Gly)	ZNF318 (R1942G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372283	NM_014345.3(ZNF318):c.5766G>T (p.Glu1922Asp)	ZNF318 (E1922D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369655	NM_014345.3(ZNF318):c.2315C>T (p.Ala772Val)	ZNF318 (A772V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365852	NM_014345.3(ZNF318):c.265T>G (p.Ser89Ala)	LOC129996503, ZNF318 (S89A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362190	NM_014345.3(ZNF318):c.2573C>T (p.Ala858Val)	ZNF318 (A858V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359164	NM_014345.3(ZNF318):c.271T>C (p.Ser91Pro)	LOC129996503, ZNF318 (S91P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357782	NM_014345.3(ZNF318):c.5111T>A (p.Phe1704Tyr)	ZNF318 (F1704Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355956	NM_014345.3(ZNF318):c.1576C>T (p.Arg526Cys)	ZNF318 (R526C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355278	NM_014345.3(ZNF318):c.3338C>A (p.Ala1113Asp)	ZNF318 (A1113D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351740	NM_014345.3(ZNF318):c.4918A>T (p.Ser1640Cys)	LOC129996502, ZNF318 (S1640C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346731	NM_014345.3(ZNF318):c.2165T>C (p.Ile722Thr)	ZNF318 (I722T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344767	NM_014345.3(ZNF318):c.1607A>G (p.Lys536Arg)	ZNF318 (K536R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333828	NM_014345.3(ZNF318):c.2778G>A (p.Met926Ile)	ZNF318 (M926I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333650	NM_014345.3(ZNF318):c.6767C>T (p.Pro2256Leu)	ZNF318 (P2256L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332628	NM_014345.3(ZNF318):c.1336C>T (p.Pro446Ser)	ZNF318 (P446S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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