12886[HGNC] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151339	GRCh38/hg38 15q15.1(chr15:41697762-42489559)x3	CAPN3, EHD4 +44 more	Copy number gain	See cases	GUncertain significance
Select item 790691	NM_001366845.3(ZNF106):c.5664+7T>G	ZNF106	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2461987	NM_001366845.3(ZNF106):c.5603C>T (p.Thr1868Ile)	ZNF106 (T1140I +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342337	NM_001366845.3(ZNF106):c.5545G>A (p.Val1849Ile)	ZNF106 (V967I +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285928	NM_001366845.3(ZNF106):c.5388A>C (p.Leu1796Phe)	ZNF106 (L1068F +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193911	NM_001366845.3(ZNF106):c.5320A>G (p.Lys1774Glu)	ZNF106 (K828E +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334884	NM_001366845.3(ZNF106):c.5246A>G (p.Asn1749Ser)	ZNF106 (N1682S +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334876	NM_001366845.3(ZNF106):c.5153C>A (p.Thr1718Asn)	ZNF106 (T764N +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268455	NM_001366845.3(ZNF106):c.5132G>A (p.Arg1711Gln)	ZNF106 (R1624Q +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193910	NM_001366845.3(ZNF106):c.5105A>G (p.Asp1702Gly)	ZNF106 (D1702G +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474428	NM_001366845.3(ZNF106):c.5030A>G (p.His1677Arg)	ZNF106 (H1677R +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334871	NM_001366845.3(ZNF106):c.5009G>T (p.Arg1670Leu)	ZNF106 (R832L +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334869	NM_001366845.3(ZNF106):c.4993A>G (p.Ile1665Val)	ZNF106 (I1665V +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193909	NM_001366845.3(ZNF106):c.4946G>T (p.Arg1649Leu)	ZNF106 (R1626L +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570300	NM_001366845.3(ZNF106):c.4946G>A (p.Arg1649Gln)	ZNF106 (R767Q +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484285	NM_001366845.3(ZNF106):c.4928G>T (p.Cys1643Phe)	ZNF106 (C1643F +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193908	NM_001366845.3(ZNF106):c.4892G>C (p.Cys1631Ser)	ZNF106 (C749S +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362464	NM_001366845.3(ZNF106):c.4892G>A (p.Cys1631Tyr)	ZNF106 (C677Y +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334872	NM_001366845.3(ZNF106):c.4854C>G (p.Asp1618Glu)	ZNF106 (D1551E +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2645238	NM_001366845.3(ZNF106):c.4803G>C (p.Leu1601=)	ZNF106	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3193907	NM_001366845.3(ZNF106):c.4762G>C (p.Gly1588Arg)	ZNF106 (G1521R +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237307	NM_001366845.3(ZNF106):c.4759A>G (p.Ile1587Val)	ZNF106 (I1500V +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3334873	NM_001366845.3(ZNF106):c.4750C>T (p.Arg1584Trp)	ZNF106 (R1497W +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193905	NM_001366845.3(ZNF106):c.4520G>A (p.Arg1507His)	ZNF106 (R553H +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221138	NM_001366845.3(ZNF106):c.4411C>G (p.Pro1471Ala)	ZNF106 (P1404A +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603220	NM_001366845.3(ZNF106):c.4247G>C (p.Gly1416Ala)	ZNF106 (G1329A +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357560	NM_001366845.3(ZNF106):c.4153C>T (p.Arg1385Trp)	ZNF106 (R547W +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334879	NM_001366845.3(ZNF106):c.4135C>G (p.Arg1379Gly)	ZNF106 (R1292G +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289334	NM_001366845.3(ZNF106):c.4127A>C (p.Lys1376Thr)	ZNF106 (K581T +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554719	NM_001366845.3(ZNF106):c.4024G>C (p.Glu1342Gln)	ZNF106 (E1319Q +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239570	NM_001366845.3(ZNF106):c.4004T>C (p.Leu1335Pro)	ZNF106 (L1268P +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2247978	NM_001366845.3(ZNF106):c.3983A>G (p.Glu1328Gly)	ZNF106 (E1261G +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517439	NM_001366845.3(ZNF106):c.3900A>T (p.Glu1300Asp)	ZNF106 (E1300D +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193904	NM_001366845.3(ZNF106):c.3658G>C (p.Val1220Leu)	ZNF106 (V1153L +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193903	NM_001366845.3(ZNF106):c.3552G>T (p.Glu1184Asp)	ZNF106 (E1161D +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334875	NM_001366845.3(ZNF106):c.3550G>A (p.Glu1184Lys)	ZNF106 (E1117K +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334882	NM_001366845.3(ZNF106):c.3521T>C (p.Leu1174Pro)	ZNF106 (L360P +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334870	NM_001366845.3(ZNF106):c.3514G>A (p.Ala1172Thr)	ZNF106 (A1105T +8 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2492180	NM_001366845.3(ZNF106):c.3449A>G (p.Asp1150Gly)	ZNF106 (D1083G +8 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3193902	NM_001366845.3(ZNF106):c.3425C>G (p.Thr1142Arg)	ZNF106 (T1119R +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193901	NM_001366845.3(ZNF106):c.3367A>C (p.Met1123Leu)	ZNF106 (M1056L +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193900	NM_001366845.3(ZNF106):c.3343C>T (p.Leu1115Phe)	ZNF106 (L1092F +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 790692	NM_001366845.3(ZNF106):c.3307G>A (p.Ala1103Thr)	ZNF106 (A1080T +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3334881	NM_001366845.3(ZNF106):c.3256C>G (p.Leu1086Val)	ZNF106 (L1019V +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593653	NM_001366845.3(ZNF106):c.3208C>T (p.Arg1070Cys)	ZNF106 (R256C +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324239	NM_001366845.3(ZNF106):c.3062C>G (p.Thr1021Arg)	ZNF106 (T207R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193899	NM_001366845.3(ZNF106):c.2987G>A (p.Ser996Asn)	ZNF106 (S973N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193898	NM_001366845.3(ZNF106):c.2937C>G (p.Asn979Lys)	ZNF106 (N912K +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193897	NM_001366845.3(ZNF106):c.2914A>T (p.Met972Leu)	ZNF106 (M244L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519952	NM_001366845.3(ZNF106):c.2900A>G (p.His967Arg)	ZNF106 (H239R +6 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2596058	NM_001366845.3(ZNF106):c.2893T>C (p.Ser965Pro)	ZNF106 (S151P +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193896	NM_001366845.3(ZNF106):c.2864C>T (p.Thr955Ile)	ZNF106 (T117I +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597344	NM_001366845.3(ZNF106):c.2847G>C (p.Arg949Ser)	ZNF106 (R154S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240634	NM_001366845.3(ZNF106):c.2834G>A (p.Arg945Gln)	ZNF106 (R150Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292685	NM_001366845.3(ZNF106):c.2697C>A (p.Phe899Leu)	ZNF106 (F171L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388957	NM_001366845.3(ZNF106):c.2686G>C (p.Val896Leu)	ZNF106 (V829L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193895	NM_001366845.3(ZNF106):c.2681C>T (p.Pro894Leu)	ZNF106 (P894L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320052	NM_001366845.3(ZNF106):c.2654A>C (p.Glu885Ala)	ZNF106 (E157A +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255113	NM_001366845.3(ZNF106):c.2642G>A (p.Arg881Gln)	ZNF106 (R43Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613863	NM_001366845.3(ZNF106):c.2632G>A (p.Ala878Thr)	ZNF106 (A150T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266079	NM_001366845.3(ZNF106):c.2593C>A (p.Gln865Lys)	ZNF106 (Q798K +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610698	NM_001366845.3(ZNF106):c.2524C>T (p.Leu842Phe)	ZNF106 (L28F +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279733	NM_001366845.3(ZNF106):c.2438A>C (p.Asn813Thr)	ZNF106 (N746T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215276	NM_001366845.3(ZNF106):c.2434G>T (p.Val812Phe)	ZNF106 (V745F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193894	NM_001366845.3(ZNF106):c.2404C>T (p.Arg802Trp)	ZNF106 (R735W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193893	NM_001366845.3(ZNF106):c.2360G>A (p.Arg787Gln)	ZNF106 (R787Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345541	NM_001366845.3(ZNF106):c.2352C>A (p.Ser784Arg)	ZNF106 (S717R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216110	NM_001366845.3(ZNF106):c.2342G>A (p.Arg781His)	ZNF106 (R714H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2280026	NM_001366845.3(ZNF106):c.2335C>T (p.Arg779Cys)	ZNF106 (R712C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334868	NM_001366845.3(ZNF106):c.2158G>A (p.Ala720Thr)	ZNF106 (A697T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2511931	NM_001366845.3(ZNF106):c.2126A>G (p.His709Arg)	ZNF106 (H642R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463678	NM_001366845.3(ZNF106):c.2015A>G (p.Gln672Arg)	ZNF106 (Q605R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527745	NM_001366845.3(ZNF106):c.2011C>T (p.Arg671Cys)	ZNF106 (R604C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273907	NM_001366845.3(ZNF106):c.1987A>G (p.Thr663Ala)	ZNF106 (T663A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470964	NM_001366845.3(ZNF106):c.1906G>A (p.Glu636Lys)	ZNF106 (E569K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193891	NM_001366845.3(ZNF106):c.1751A>G (p.Asn584Ser)	ZNF106 (N584S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193890	NM_001366845.3(ZNF106):c.1676G>A (p.Arg559Gln)	ZNF106 (R559Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3193889	NM_001366845.3(ZNF106):c.1670C>A (p.Thr557Asn)	ZNF106 (T557N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288139	NM_001366845.3(ZNF106):c.1669A>G (p.Thr557Ala)	ZNF106 (T490A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193887	NM_001366845.3(ZNF106):c.1573T>C (p.Tyr525His)	ZNF106 (Y458H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193886	NM_001366845.3(ZNF106):c.1565A>G (p.His522Arg)	ZNF106 (H522R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459944	NM_001366845.3(ZNF106):c.1531A>G (p.Asn511Asp)	ZNF106 (N444D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2343733	NM_001366845.3(ZNF106):c.1513T>C (p.Ser505Pro)	ZNF106 (S482P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334883	NM_001366845.3(ZNF106):c.1429C>G (p.Leu477Val)	ZNF106 (L454V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193885	NM_001366845.3(ZNF106):c.1348G>A (p.Glu450Lys)	ZNF106 (E383K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193883	NM_001366845.3(ZNF106):c.1288A>C (p.Lys430Gln)	ZNF106 (K430Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467476	NM_001366845.3(ZNF106):c.1261C>T (p.Arg421Cys)	ZNF106 (R421C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456252	NM_001366845.3(ZNF106):c.1248A>C (p.Gln416His)	ZNF106 (Q349H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620952	NM_001366845.3(ZNF106):c.1139C>T (p.Thr380Ile)	ZNF106 (T313I +2 more)	Single nucleotide variant (intron variant +1 more)	not specified	GUncertain significance
Select item 2299831	NM_001366845.3(ZNF106):c.1130C>T (p.Ser377Phe)	ZNF106 (S310F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193882	NM_001366845.3(ZNF106):c.1091C>T (p.Ala364Val)	ZNF106 (A297V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2681655	NM_001366845.3(ZNF106):c.1090G>A (p.Ala364Thr)	ZNF106 (A297T +2 more)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 3193914	NM_001366845.3(ZNF106):c.1013A>C (p.Asn338Thr)	ZNF106 (N271T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258883	NM_001366845.3(ZNF106):c.974C>T (p.Thr325Ile)	ZNF106 (T325I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350090	NM_001366845.3(ZNF106):c.914G>A (p.Arg305Gln)	ZNF106 (R282Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553872	NM_001366845.3(ZNF106):c.880A>G (p.Asn294Asp)	ZNF106 (N227D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492548	NM_001366845.3(ZNF106):c.758G>A (p.Arg253His)	ZNF106 (R186H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269588	NM_001366845.3(ZNF106):c.758G>T (p.Arg253Leu)	ZNF106 (R253L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334874	NM_001366845.3(ZNF106):c.757C>T (p.Arg253Cys)	ZNF106 (R186C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334878	NM_001366845.3(ZNF106):c.735C>T (p.Asn245=)	ZNF106	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign

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