"Ambry Genetics"[submitter] AND "NCOR1"[gene] - ClinVar

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Items: 62

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2610718	NM_006311.4(NCOR1):c.7202T>C (p.Ile2401Thr)	NCOR1, TTC19 (I2401T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242519	NM_006311.4(NCOR1):c.7166C>T (p.Thr2389Ile)	TTC19, NCOR1 (T2286I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302325	NM_006311.4(NCOR1):c.7027G>C (p.Gly2343Arg)	NCOR1, TTC19 (G2240R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2306699	NM_006311.4(NCOR1):c.6939C>A (p.Asp2313Glu)	NCOR1, TTC19 (D2313E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236275	NM_006311.4(NCOR1):c.6833A>G (p.Lys2278Arg)	NCOR1, TTC19 (K2175R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495258	NM_006311.4(NCOR1):c.6817G>A (p.Gly2273Arg)	NCOR1, TTC19 (G2170R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2356539	NM_006311.4(NCOR1):c.6773C>G (p.Ala2258Gly)	TTC19, NCOR1 (A2258G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2490395	NM_006311.4(NCOR1):c.6517G>A (p.Ala2173Thr)	NCOR1 (A2173T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300913	NM_006311.4(NCOR1):c.6371T>C (p.Leu2124Pro)	NCOR1 (L2021P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2478170	NM_006311.4(NCOR1):c.6269C>T (p.Ser2090Phe)	NCOR1 (S1987F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465065	NM_006311.4(NCOR1):c.6209C>T (p.Ser2070Leu)	NCOR1 (S1967L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2600335	NM_006311.4(NCOR1):c.6094C>G (p.Pro2032Ala)	NCOR1 (P2032A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533131	NM_006311.4(NCOR1):c.6073T>C (p.Ser2025Pro)	NCOR1 (S1922P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2555745	NM_006311.4(NCOR1):c.5962A>C (p.Lys1988Gln)	NCOR1 (K1988Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2213418	NM_006311.4(NCOR1):c.5954C>T (p.Pro1985Leu)	NCOR1 (P1985L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2408754	NM_006311.4(NCOR1):c.5939G>A (p.Ser1980Asn)	NCOR1 (S1980N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261991	NM_006311.4(NCOR1):c.5717A>G (p.Asp1906Gly)	NCOR1 (D1906G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2340283	NM_006311.4(NCOR1):c.5611C>G (p.Leu1871Val)	NCOR1 (L1871V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2570308	NM_006311.4(NCOR1):c.5299A>G (p.Met1767Val)	NCOR1 (M1783V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2221939	NM_006311.4(NCOR1):c.5177G>A (p.Arg1726Gln)	NCOR1 (R1726Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242442	NM_006311.4(NCOR1):c.5152C>T (p.Arg1718Trp)	NCOR1 (R1734W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328635	NM_006311.4(NCOR1):c.5149G>A (p.Glu1717Lys)	NCOR1 (E1733K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351621	NM_006311.4(NCOR1):c.5086G>C (p.Ala1696Pro)	NCOR1 (A1712P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2311268	NM_006311.4(NCOR1):c.4888G>A (p.Asp1630Asn)	NCOR1 (D1630N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2538809	NM_006311.4(NCOR1):c.4724A>G (p.His1575Arg)	NCOR1 (H1575R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348112	NM_006311.4(NCOR1):c.4592C>T (p.Ala1531Val)	NCOR1 (A1531V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2229431	NM_006311.4(NCOR1):c.4472C>T (p.Thr1491Ile)	NCOR1 (T1491I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2273151	NM_006311.4(NCOR1):c.4397C>T (p.Ala1466Val)	NCOR1 (A1466V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301854	NM_006311.4(NCOR1):c.4355T>C (p.Val1452Ala)	NCOR1 (V1452A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2214070	NM_006311.4(NCOR1):c.4244G>A (p.Arg1415His)	NCOR1 (R1415H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2297664	NM_006311.4(NCOR1):c.3968C>T (p.Pro1323Leu)	NCOR1 (P1323L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2468826	NM_006311.4(NCOR1):c.3724A>G (p.Ser1242Gly)	NCOR1 (S1242G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588473	NM_006311.4(NCOR1):c.3671A>G (p.Asn1224Ser)	NCOR1 (N1240S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488269	NM_006311.4(NCOR1):c.3640G>A (p.Gly1214Ser)	NCOR1 (G1214S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2336917	NM_006311.4(NCOR1):c.3497C>G (p.Thr1166Ser)	NCOR1 (T1182S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2287859	NM_006311.4(NCOR1):c.3415A>G (p.Ile1139Val)	NCOR1 (I1155V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2255289	NM_006311.4(NCOR1):c.3316A>G (p.Lys1106Glu)	NCOR1 (K1122E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2553919	NM_006311.4(NCOR1):c.3301A>G (p.Thr1101Ala)	NCOR1 (T1101A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334774	NM_006311.4(NCOR1):c.3128C>T (p.Thr1043Ile)	NCOR1 (T1043I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330638	NM_006311.4(NCOR1):c.3083G>A (p.Arg1028Gln)	NCOR1 (R1044Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2486241	NM_006311.4(NCOR1):c.3073C>T (p.Pro1025Ser)	NCOR1 (P1041S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2408898	NM_006311.4(NCOR1):c.3064G>A (p.Val1022Ile)	NCOR1 (V1022I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2219048	NM_006311.4(NCOR1):c.2890A>G (p.Ile964Val)	NCOR1 (I980V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2481133	NM_006311.4(NCOR1):c.2527G>A (p.Glu843Lys)	NCOR1 (E750K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2557272	NM_006311.4(NCOR1):c.2510A>G (p.Glu837Gly)	NCOR1 (E837G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2213893	NM_006311.4(NCOR1):c.2411G>A (p.Ser804Asn)	NCOR1 (S804N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2219681	NM_006311.4(NCOR1):c.2303C>T (p.Ala768Val)	NCOR1 (A675V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2281844	NM_006311.4(NCOR1):c.2270C>T (p.Thr757Met)	NCOR1 (T773M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527894	NM_006311.4(NCOR1):c.2030A>G (p.Asn677Ser)	NCOR1 (N568S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2570260	NM_006311.4(NCOR1):c.1838C>T (p.Pro613Leu)	NCOR1 (P504L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2241770	NM_006311.4(NCOR1):c.1765A>G (p.Met589Val)	NCOR1 (M589V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2603465	NM_006311.4(NCOR1):c.1744A>G (p.Lys582Glu)	NCOR1 (K473E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2464395	NM_006311.4(NCOR1):c.1703C>T (p.Thr568Ile)	NCOR1 (T459I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2316357	NM_006311.4(NCOR1):c.1327C>G (p.His443Asp)	NCOR1 (H443D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2321851	NM_006311.4(NCOR1):c.739G>A (p.Ala247Thr)	NCOR1 (A138T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2218092	NM_006311.4(NCOR1):c.422C>T (p.Ala141Val)	NCOR1 (A141V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2207169	NM_006311.4(NCOR1):c.374C>T (p.Ala125Val)	NCOR1 (A125V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2257695	NM_006311.4(NCOR1):c.290C>T (p.Ser97Phe)	NCOR1 (S97F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2323033	NM_006311.4(NCOR1):c.272C>T (p.Pro91Leu)	NCOR1 (P91L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2272678	NM_006311.4(NCOR1):c.131G>A (p.Arg44His)	NCOR1 (R44H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2532794	NM_006311.4(NCOR1):c.130C>T (p.Arg44Cys)	NCOR1 (R44C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2508691	NM_006311.4(NCOR1):c.49C>G (p.Gln17Glu)	NCOR1 (Q17E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 62