ClinVar for Gene (Select 9612) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3298936	NM_006312.6(NCOR2):c.2024A>G (p.Lys675Arg)	NCOR2 (K675R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298935	NM_006312.6(NCOR2):c.6391A>G (p.Thr2131Ala)	NCOR2 (T2121A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298934	NM_006312.6(NCOR2):c.3397C>T (p.Leu1133Phe)	NCOR2 (L1133F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298933	NM_006312.6(NCOR2):c.5537G>A (p.Ser1846Asn)	NCOR2 (S1836N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298932	NM_006312.6(NCOR2):c.7313G>A (p.Arg2438His)	NCOR2 (R2428H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298930	NM_006312.6(NCOR2):c.6533G>A (p.Ser2178Asn)	NCOR2 (S2178N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298929	NM_006312.6(NCOR2):c.6550C>T (p.Pro2184Ser)	NCOR2 (P2174S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298928	NM_006312.6(NCOR2):c.4543G>A (p.Ala1515Thr)	NCOR2 (A1505T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298927	NM_006312.6(NCOR2):c.5927C>G (p.Ser1976Trp)	NCOR2 (S1966W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298926	NM_006312.6(NCOR2):c.6040T>A (p.Ser2014Thr)	NCOR2 (S2014T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298925	NM_006312.6(NCOR2):c.5284C>A (p.Pro1762Thr)	NCOR2 (P1752T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298924	NM_006312.6(NCOR2):c.1721G>T (p.Ser574Ile)	NCOR2 (S573I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298923	NM_006312.6(NCOR2):c.5270G>T (p.Arg1757Leu)	NCOR2 (R1747L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298922	NM_006312.6(NCOR2):c.6142G>A (p.Glu2048Lys)	NCOR2 (E2048K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298921	NM_006312.6(NCOR2):c.461C>T (p.Pro154Leu)	NCOR2 (P154L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298919	NM_006312.6(NCOR2):c.4154C>T (p.Pro1385Leu)	NCOR2 (P1375L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298918	NM_006312.6(NCOR2):c.3122A>C (p.Lys1041Thr)	NCOR2 (K1041T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298917	NM_006312.6(NCOR2):c.2621C>T (p.Pro874Leu)	NCOR2 (P856L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298916	NM_006312.6(NCOR2):c.110T>C (p.Val37Ala)	NCOR2 (V37A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298915	NM_006312.6(NCOR2):c.2090C>T (p.Pro697Leu)	NCOR2 (P696L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298914	NM_006312.6(NCOR2):c.3095A>C (p.Lys1032Thr)	NCOR2 (K1032T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298913	NM_006312.6(NCOR2):c.4558G>A (p.Gly1520Ser)	NCOR2 (G1520S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298912	NM_006312.6(NCOR2):c.5117G>A (p.Arg1706Gln)	NCOR2 (R1696Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298911	NM_006312.6(NCOR2):c.5839C>T (p.Arg1947Trp)	NCOR2 (R1947W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298910	NM_006312.6(NCOR2):c.7409C>T (p.Ala2470Val)	NCOR2 (A2470V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298909	NM_006312.6(NCOR2):c.1370T>A (p.Phe457Tyr)	NCOR2 (F456Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298908	NM_006312.6(NCOR2):c.2627A>G (p.Lys876Arg)	NCOR2 (K858R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298907	NM_006312.6(NCOR2):c.3005C>T (p.Pro1002Leu)	NCOR2 (P1002L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298906	NM_006312.6(NCOR2):c.6674C>T (p.Pro2225Leu)	NCOR2 (P2225L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298905	NM_006312.6(NCOR2):c.1017G>T (p.Glu339Asp)	NCOR2 (E339D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298904	NM_006312.6(NCOR2):c.5421T>G (p.Asp1807Glu)	NCOR2 (D1807E +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3298903	NM_006312.6(NCOR2):c.5447C>T (p.Thr1816Met)	NCOR2 (T1806M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185205	NM_006312.6(NCOR2):c.7483T>C (p.Trp2495Arg)	NCOR2 (W2495R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185202	NM_006312.6(NCOR2):c.7477C>T (p.His2493Tyr)	NCOR2 (H2483Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185198	NM_006312.6(NCOR2):c.7448C>T (p.Ala2483Val)	NCOR2 (A2427V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185187	NM_006312.6(NCOR2):c.7333C>T (p.Arg2445Cys)	NCOR2 (R2389C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185176	NM_006312.6(NCOR2):c.7004C>G (p.Thr2335Ser)	NCOR2 (T2325S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185172	NM_006312.6(NCOR2):c.6971A>G (p.Tyr2324Cys)	NCOR2 (Y2314C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3185141	NM_006312.6(NCOR2):c.6320C>T (p.Pro2107Leu)	NCOR2 (P2097L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185133	NM_006312.6(NCOR2):c.6190G>A (p.Asp2064Asn)	NCOR2 (D2054N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185125	NM_006312.6(NCOR2):c.6137G>A (p.Ser2046Asn)	NCOR2 (S2046N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185122	NM_006312.6(NCOR2):c.6047C>T (p.Ser2016Leu)	NCOR2 (S2016L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185119	NM_006312.6(NCOR2):c.6017C>T (p.Pro2006Leu)	NCOR2 (P1996L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185108	NM_006312.6(NCOR2):c.5978G>A (p.Arg1993His)	NCOR2 (R1993H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185102	NM_006312.6(NCOR2):c.5974G>A (p.Ala1992Thr)	NCOR2 (A1982T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185097	NM_006312.6(NCOR2):c.5846G>A (p.Arg1949Gln)	NCOR2 (R1949Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185093	NM_006312.6(NCOR2):c.5840G>A (p.Arg1947Gln)	NCOR2 (R1937Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185079	NM_006312.6(NCOR2):c.5710G>A (p.Val1904Ile)	NCOR2 (V1894I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185075	NM_006312.6(NCOR2):c.5656G>A (p.Ala1886Thr)	NCOR2 (A1876T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185048	NM_006312.6(NCOR2):c.5549C>G (p.Ser1850Cys)	NCOR2 (S1850C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185038	NM_006312.6(NCOR2):c.5545G>T (p.Ala1849Ser)	NCOR2 (A1839S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185025	NM_006312.6(NCOR2):c.5455A>G (p.Thr1819Ala)	NCOR2 (T1819A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185018	NM_006312.6(NCOR2):c.5422C>T (p.Arg1808Trp)	NCOR2 (R1808W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185010	NM_006312.6(NCOR2):c.5416C>T (p.Arg1806Trp)	NCOR2 (R1806W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185002	NM_006312.6(NCOR2):c.5311C>T (p.Arg1771Cys)	NCOR2 (R1771C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184993	NM_006312.6(NCOR2):c.5257A>T (p.Thr1753Ser)	NCOR2 (T1743S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184986	NM_006312.6(NCOR2):c.5237C>T (p.Pro1746Leu)	NCOR2 (P1736L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184962	NM_006312.6(NCOR2):c.5107A>G (p.Met1703Val)	NCOR2 (M1693V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184956	NM_006312.6(NCOR2):c.5104G>C (p.Ala1702Pro)	NCOR2 (A1692P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184943	NM_006312.6(NCOR2):c.4933G>A (p.Ala1645Thr)	NCOR2 (A1635T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184937	NM_006312.6(NCOR2):c.4832A>G (p.Tyr1611Cys)	NCOR2 (Y1601C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184933	NM_006312.6(NCOR2):c.4822A>G (p.Ile1608Val)	NCOR2 (I1598V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184925	NM_006312.6(NCOR2):c.4798G>A (p.Val1600Met)	NCOR2 (V1590M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184918	NM_006312.6(NCOR2):c.4777G>A (p.Ala1593Thr)	NCOR2 (A1583T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184900	NM_006312.6(NCOR2):c.4628A>G (p.Tyr1543Cys)	NCOR2 (Y1533C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184888	NM_006312.6(NCOR2):c.4573G>A (p.Gly1525Ser)	NCOR2 (G1525S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184859	NM_006312.6(NCOR2):c.4448C>T (p.Thr1483Met)	NCOR2 (T1483M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184858	NM_006312.6(NCOR2):c.4432G>A (p.Gly1478Ser)	NCOR2 (G1478S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184854	NM_006312.6(NCOR2):c.4429A>T (p.Ile1477Phe)	NCOR2 (I1477F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184842	NM_006312.6(NCOR2):c.4226C>T (p.Pro1409Leu)	NCOR2 (P1399L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184837	NM_006312.6(NCOR2):c.4138C>T (p.Arg1380Trp)	NCOR2 (R1380W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184830	NM_006312.6(NCOR2):c.3994G>C (p.Gly1332Arg)	NCOR2 (G1322R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184827	NM_006312.6(NCOR2):c.3961G>A (p.Ala1321Thr)	LOC124849275, NCOR2 (A1311T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184826	NM_006312.6(NCOR2):c.3916G>A (p.Ala1306Thr)	LOC124849275, NCOR2 (A1296T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184823	NM_006312.6(NCOR2):c.3899C>T (p.Pro1300Leu)	LOC124849275, NCOR2 (P1290L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184813	NM_006312.6(NCOR2):c.3765G>C (p.Leu1255Phe)	NCOR2 (L1255F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184810	NM_006312.6(NCOR2):c.3739A>G (p.Ile1247Val)	NCOR2 (I1247V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184780	NM_006312.6(NCOR2):c.3448A>G (p.Met1150Val)	NCOR2 (M1150V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184756	NM_006312.6(NCOR2):c.3173C>A (p.Pro1058His)	NCOR2 (P1048H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184753	NM_006312.6(NCOR2):c.3128C>G (p.Pro1043Arg)	NCOR2 (P1033R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184748	NM_006312.6(NCOR2):c.3091G>A (p.Asp1031Asn)	NCOR2 (D1013N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184737	NM_006312.6(NCOR2):c.3061G>A (p.Gly1021Ser)	NCOR2 (G1003S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184723	NM_006312.6(NCOR2):c.2959G>A (p.Glu987Lys)	NCOR2 (E969K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184719	NM_006312.6(NCOR2):c.2951C>A (p.Pro984His)	NCOR2 (P966H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184708	NM_006312.6(NCOR2):c.2861A>G (p.Asn954Ser)	NCOR2 (N954S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3184702	NM_006312.6(NCOR2):c.2686A>G (p.Lys896Glu)	NCOR2 (K878E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184699	NM_006312.6(NCOR2):c.2648C>T (p.Ala883Val)	NCOR2 (A883V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184689	NM_006312.6(NCOR2):c.2539G>A (p.Ala847Thr)	NCOR2 (A847T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184682	NM_006312.6(NCOR2):c.2434C>A (p.Pro812Thr)	NCOR2 (P812T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184679	NM_006312.6(NCOR2):c.2420C>T (p.Thr807Met)	NCOR2 (T789M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184674	NM_006312.6(NCOR2):c.2245G>A (p.Glu749Lys)	NCOR2 (E731K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184668	NM_006312.6(NCOR2):c.2128G>T (p.Val710Leu)	NCOR2 (V709L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184665	NM_006312.6(NCOR2):c.2063C>T (p.Ala688Val)	NCOR2 (A688V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184661	NM_006312.6(NCOR2):c.2042G>A (p.Arg681Lys)	NCOR2 (R681K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184659	NM_006312.6(NCOR2):c.2000A>G (p.Gln667Arg)	NCOR2 (Q666R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184652	NM_006312.6(NCOR2):c.179A>C (p.Gln60Pro)	NCOR2 (Q60P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060828	NM_006312.6(NCOR2):c.1496AGC[14] (p.Gln510_Pro511insGlnGln)	NCOR2	Microsatellite	NCOR2-related disorder	GBenign
Select item 3060702	NM_006312.6(NCOR2):c.1329-4G>A	NCOR2	Single nucleotide variant (intron variant)	NCOR2-related disorder	GBenign
Select item 3060500	NM_006312.6(NCOR2):c.4623G>A (p.Leu1541=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related disorder	GBenign
Select item 3060147	NM_006312.6(NCOR2):c.2715A>T (p.Thr905=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related disorder	GBenign

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