ClinVar for Gene (Select 9612) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3403674	NM_006312.6(NCOR2):c.3193G>C (p.Ala1065Pro)	NCOR2 (A1055P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403673	NM_006312.6(NCOR2):c.2254C>G (p.Pro752Ala)	NCOR2 (P752A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403672	NM_006312.6(NCOR2):c.5251C>T (p.Pro1751Ser)	NCOR2 (P1741S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403671	NM_006312.6(NCOR2):c.6445C>T (p.Pro2149Ser)	NCOR2 (P2149S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403670	NM_006312.6(NCOR2):c.4204C>G (p.Leu1402Val)	NCOR2 (L1392V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403668	NM_006312.6(NCOR2):c.3764T>C (p.Leu1255Ser)	NCOR2 (L1245S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403667	NM_006312.6(NCOR2):c.6358G>A (p.Ala2120Thr)	NCOR2 (A2120T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3403666	NM_006312.6(NCOR2):c.5857G>A (p.Gly1953Ser)	NCOR2 (G1943S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403665	NM_006312.6(NCOR2):c.6250C>T (p.Arg2084Trp)	NCOR2 (R2084W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403664	NM_006312.6(NCOR2):c.5927C>T (p.Ser1976Leu)	NCOR2 (S1966L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403663	NM_006312.6(NCOR2):c.5378C>T (p.Ser1793Leu)	NCOR2 (S1783L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403662	NM_006312.6(NCOR2):c.2744G>A (p.Ser915Asn)	NCOR2 (S897N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403661	NM_006312.6(NCOR2):c.1088T>C (p.Met363Thr)	NCOR2 (M362T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403660	NM_006312.6(NCOR2):c.2134G>A (p.Gly712Arg)	NCOR2 (G711R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403659	NM_006312.6(NCOR2):c.3283G>A (p.Val1095Ile)	NCOR2 (V1095I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403657	NM_006312.6(NCOR2):c.4147A>T (p.Thr1383Ser)	NCOR2 (T1373S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403656	NM_006312.6(NCOR2):c.1622A>T (p.Asp541Val)	NCOR2 (D541V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403655	NM_006312.6(NCOR2):c.6664G>A (p.Val2222Met)	NCOR2 (V2222M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403654	NM_006312.6(NCOR2):c.6163C>G (p.Pro2055Ala)	NCOR2 (P2045A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403653	NM_006312.6(NCOR2):c.6424C>G (p.Gln2142Glu)	NCOR2 (Q2142E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403652	NM_006312.6(NCOR2):c.139C>T (p.Arg47Cys)	NCOR2 (R47C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403651	NM_006312.6(NCOR2):c.3697A>G (p.Thr1233Ala)	NCOR2 (T1223A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403650	NM_006312.6(NCOR2):c.610G>T (p.Ala204Ser)	LOC106783497, NCOR2 (A204S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403649	NM_006312.6(NCOR2):c.2077G>A (p.Glu693Lys)	NCOR2 (E693K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403648	NM_006312.6(NCOR2):c.2956C>T (p.Arg986Trp)	NCOR2 (R968W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403646	NM_006312.6(NCOR2):c.4739C>G (p.Ser1580Cys)	NCOR2 (S1580C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403645	NM_006312.6(NCOR2):c.3154G>A (p.Gly1052Ser)	NCOR2 (G1052S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403644	NM_006312.6(NCOR2):c.359C>T (p.Pro120Leu)	NCOR2 (P120L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403643	NM_006312.6(NCOR2):c.3385A>G (p.Met1129Val)	NCOR2 (M1119V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403642	NM_006312.6(NCOR2):c.4130T>G (p.Leu1377Arg)	NCOR2 (L1377R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403641	NM_006312.6(NCOR2):c.4619C>T (p.Pro1540Leu)	NCOR2 (P1530L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403640	NM_006312.6(NCOR2):c.3355G>A (p.Glu1119Lys)	NCOR2 (E1109K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403639	NM_006312.6(NCOR2):c.5588G>T (p.Arg1863Leu)	NCOR2 (R1863L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403638	NM_006312.6(NCOR2):c.4621C>G (p.Leu1541Val)	NCOR2 (L1531V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403636	NM_006312.6(NCOR2):c.5265G>A (p.Met1755Ile)	NCOR2 (M1745I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403635	NM_006312.6(NCOR2):c.5168A>G (p.Asn1723Ser)	NCOR2 (N1713S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403634	NM_006312.6(NCOR2):c.614C>T (p.Ala205Val)	LOC106783497, NCOR2 (A205V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403633	NM_006312.6(NCOR2):c.6683T>C (p.Met2228Thr)	NCOR2 (M2228T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403632	NM_006312.6(NCOR2):c.6157G>A (p.Val2053Ile)	NCOR2 (V2053I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403631	NM_006312.6(NCOR2):c.4861G>A (p.Val1621Met)	NCOR2 (V1611M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403630	NM_006312.6(NCOR2):c.1795C>G (p.Gln599Glu)	NCOR2 (Q599E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403629	NM_006312.6(NCOR2):c.2468C>T (p.Pro823Leu)	NCOR2 (P823L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403628	NM_006312.6(NCOR2):c.2117A>C (p.Glu706Ala)	NCOR2 (E706A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403626	NM_006312.6(NCOR2):c.5261C>A (p.Ala1754Asp)	NCOR2 (A1754D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403625	NM_006312.6(NCOR2):c.1292T>G (p.Met431Arg)	NCOR2 (M430R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403624	NM_006312.6(NCOR2):c.4486G>A (p.Ala1496Thr)	NCOR2 (A1496T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403623	NM_006312.6(NCOR2):c.6461C>T (p.Ala2154Val)	NCOR2 (A2144V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403622	NM_006312.6(NCOR2):c.4091T>C (p.Val1364Ala)	NCOR2 (V1364A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403621	NM_006312.6(NCOR2):c.4016G>A (p.Arg1339Gln)	NCOR2 (R1329Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403620	NM_006312.6(NCOR2):c.6703C>T (p.Arg2235Trp)	NCOR2 (R2225W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403619	NM_006312.6(NCOR2):c.4163C>T (p.Pro1388Leu)	NCOR2 (P1388L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403618	NM_006312.6(NCOR2):c.7336G>A (p.Val2446Met)	NCOR2 (V2390M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403616	NM_006312.6(NCOR2):c.7178C>G (p.Ser2393Trp)	NCOR2 (S2383W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3403615	NM_006312.6(NCOR2):c.3178C>T (p.Arg1060Cys)	NCOR2 (R1050C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403614	NM_006312.6(NCOR2):c.6985G>A (p.Val2329Met)	NCOR2 (V2319M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403613	NM_006312.6(NCOR2):c.457C>T (p.Pro153Ser)	NCOR2 (P153S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403612	NM_006312.6(NCOR2):c.4916G>A (p.Arg1639His)	NCOR2 (R1639H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403610	NM_006312.6(NCOR2):c.7316G>A (p.Arg2439Gln)	NCOR2 (R2383Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403609	NM_006312.6(NCOR2):c.3059G>A (p.Arg1020Gln)	NCOR2 (R1002Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3403608	NM_006312.6(NCOR2):c.6911G>A (p.Ser2304Asn)	NCOR2 (S2294N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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

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