ClinVar for Gene (Select 9611) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3352993	NM_006311.4(NCOR1):c.5387+7C>T	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related disorder	GLikely benign
Select item 3350077	NM_006311.4(NCOR1):c.4900G>A (p.Gly1634Arg)	NCOR1 (G1634R +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GUncertain significance
Select item 3350035	NM_006311.4(NCOR1):c.6798_6800del (p.Ile2267del)	NCOR1, TTC19 (I2164del +1 more)	Deletion (inframe_deletion)	NCOR1-related disorder	GUncertain significance
Select item 3347824	NM_006311.4(NCOR1):c.3079A>G (p.Thr1027Ala)	NCOR1 (T1027A +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GUncertain significance
Select item 3298902	NM_006311.4(NCOR1):c.2371G>C (p.Glu791Gln)	NCOR1 (E807Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298901	NM_006311.4(NCOR1):c.6976C>A (p.Leu2326Met)	NCOR1, TTC19 (L2223M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298900	NM_006311.4(NCOR1):c.4772T>C (p.Leu1591Pro)	NCOR1 (L1591P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298899	NM_006311.4(NCOR1):c.4169T>C (p.Phe1390Ser)	NCOR1 (F1406S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298898	NM_006311.4(NCOR1):c.6253C>T (p.Pro2085Ser)	NCOR1 (P1982S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298897	NM_006311.4(NCOR1):c.4493T>C (p.Met1498Thr)	NCOR1 (M1514T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298896	NM_006311.4(NCOR1):c.6095C>T (p.Pro2032Leu)	NCOR1 (P1929L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298895	NM_006311.4(NCOR1):c.6277G>A (p.Val2093Met)	NCOR1 (V1990M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298894	NM_006311.4(NCOR1):c.317C>T (p.Ser106Leu)	NCOR1 (S106L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298893	NM_006311.4(NCOR1):c.3228A>C (p.Gln1076His)	NCOR1 (Q1076H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298892	NM_006311.4(NCOR1):c.178C>G (p.Gln60Glu)	NCOR1 (Q60E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298891	NM_006311.4(NCOR1):c.1934G>A (p.Arg645His)	NCOR1 (R536H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298890	NM_006311.4(NCOR1):c.1526C>T (p.Ser509Leu)	NCOR1 (S509L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298889	NM_006311.4(NCOR1):c.3579A>C (p.Glu1193Asp)	NCOR1 (E1209D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298888	NM_006311.4(NCOR1):c.5128G>A (p.Ala1710Thr)	NCOR1 (A1710T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184628	NM_006311.4(NCOR1):c.758T>A (p.Ile253Asn)	NCOR1 (I253N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184626	NM_006311.4(NCOR1):c.746A>C (p.Glu249Ala)	NCOR1 (E140A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184619	NM_006311.4(NCOR1):c.7040C>T (p.Thr2347Met)	NCOR1, TTC19 (T2244M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184614	NM_006311.4(NCOR1):c.6957A>G (p.Gly2319=)	NCOR1, TTC19	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3184607	NM_006311.4(NCOR1):c.6934G>A (p.Gly2312Arg)	NCOR1, TTC19 (G2312R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184597	NM_006311.4(NCOR1):c.6736T>G (p.Ser2246Ala)	NCOR1, TTC19 (S2246A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184588	NM_006311.4(NCOR1):c.6143T>C (p.Leu2048Pro)	NCOR1 (L1945P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184583	NM_006311.4(NCOR1):c.6053G>A (p.Arg2018Gln)	NCOR1 (R2018Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184576	NM_006311.4(NCOR1):c.6005C>T (p.Ala2002Val)	NCOR1 (A2002V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184565	NM_006311.4(NCOR1):c.5840C>T (p.Ala1947Val)	NCOR1 (A1947V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3184556	NM_006311.4(NCOR1):c.5657C>G (p.Ala1886Gly)	NCOR1 (A1886G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3184552	NM_006311.4(NCOR1):c.5632G>A (p.Val1878Ile)	NCOR1 (V1878I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3184545	NM_006311.4(NCOR1):c.5407C>T (p.Pro1803Ser)	NCOR1 (P1819S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184532	NM_006311.4(NCOR1):c.5110A>G (p.Thr1704Ala)	NCOR1 (T1720A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184517	NM_006311.4(NCOR1):c.4813G>A (p.Ala1605Thr)	NCOR1 (A1605T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184508	NM_006311.4(NCOR1):c.4570A>T (p.Thr1524Ser)	NCOR1 (T1524S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184491	NM_006311.4(NCOR1):c.3980C>T (p.Ala1327Val)	NCOR1 (A1327V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184485	NM_006311.4(NCOR1):c.3941A>T (p.Tyr1314Phe)	NCOR1 (Y1314F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184464	NM_006311.4(NCOR1):c.3491C>G (p.Ser1164Cys)	NCOR1 (S1180C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184455	NM_006311.4(NCOR1):c.3256A>G (p.Ile1086Val)	NCOR1 (I1086V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184432	NM_006311.4(NCOR1):c.2993A>G (p.Lys998Arg)	NCOR1 (K1014R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184423	NM_006311.4(NCOR1):c.2870A>T (p.Tyr957Phe)	NCOR1 (Y864F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184418	NM_006311.4(NCOR1):c.2776G>C (p.Asp926His)	NCOR1 (D833H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184414	NM_006311.4(NCOR1):c.2552A>T (p.Glu851Val)	NCOR1 (E758V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184398	NM_006311.4(NCOR1):c.2249C>T (p.Ala750Val)	NCOR1 (A657V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3184388	NM_006311.4(NCOR1):c.1681A>G (p.Thr561Ala)	NCOR1 (T452A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184386	NM_006311.4(NCOR1):c.1672G>A (p.Ala558Thr)	NCOR1 (A558T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184384	NM_006311.4(NCOR1):c.1417G>C (p.Asp473His)	NCOR1 (D364H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063519	GRCh37/hg19 17p11.2(chr17:16096240-16317075)x3	CENPV, NCOR1 +2 more	Copy number gain	not specified	GUncertain significance
Select item 3063517	GRCh37/hg19 17p12-11.2(chr17:15759103-20564268)x1	ADORA2B, AKAP10 +61 more	Copy number loss	not specified	GPathogenic
Select item 3063493	GRCh37/hg19 17p12-11.2(chr17:15872060-16909718)x3	ADORA2B, CCDC144A +11 more	Copy number gain	not specified	GUncertain significance
Select item 3063486	GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	ABR, ACADVL +329 more	Copy number gain	not specified	GPathogenic
Select item 3059996	NM_006311.4(NCOR1):c.4153-5T>A	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related disorder	GBenign
Select item 3058498	NM_006311.4(NCOR1):c.6678G>A (p.Met2226Ile)	NCOR1 (M2123I +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GLikely benign
Select item 3056547	NM_006311.4(NCOR1):c.3436C>A (p.Arg1146=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3056111	NM_006311.4(NCOR1):c.5986GTT[1] (p.Val1997del)	NCOR1 (V1894del +1 more)	Microsatellite	NCOR1-related disorder	GBenign
Select item 3055775	NM_006311.4(NCOR1):c.2445C>T (p.Pro815=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3055358	NM_006311.4(NCOR1):c.2366G>C (p.Ser789Thr)	NCOR1 (S696T +2 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GLikely benign
Select item 3054351	NM_006311.4(NCOR1):c.6010+6T>C	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related disorder	GLikely benign
Select item 3052795	NM_006311.4(NCOR1):c.675T>A (p.Pro225=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3052555	NM_006311.4(NCOR1):c.180G>A (p.Gln60=)	NCOR1	Single nucleotide variant (synonymous variant +1 more)	NCOR1-related disorder	GBenign
Select item 3050696	NM_006311.4(NCOR1):c.6441C>T (p.Tyr2147=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3049993	NM_006311.4(NCOR1):c.1488G>A (p.Gly496=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3049594	NM_006311.4(NCOR1):c.1352+10A>G	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related disorder	GLikely benign
Select item 3049019	NM_006311.4(NCOR1):c.6312A>G (p.Glu2104=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3042406	NM_006311.4(NCOR1):c.2250G>A (p.Ala750=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3039988	NM_006311.4(NCOR1):c.768T>C (p.Gly256=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3038963	NM_006311.4(NCOR1):c.5076G>A (p.Pro1692=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3038527	NM_006311.4(NCOR1):c.3309C>T (p.Pro1103=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3035259	NM_006311.4(NCOR1):c.3686G>A (p.Arg1229Gln)	NCOR1 (R1229Q +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GLikely benign
Select item 3035132	NM_006311.4(NCOR1):c.3338G>A (p.Arg1113Gln)	NCOR1 (R1113Q +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GBenign
Select item 3034508	NM_006311.4(NCOR1):c.2058T>C (p.Thr686=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3033586	NM_006311.4(NCOR1):c.2744T>G (p.Leu915Arg)	NCOR1 (L822R +2 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GLikely benign
Select item 3031103	NM_006311.4(NCOR1):c.4505C>T (p.Thr1502Ile)	NCOR1 (T1502I +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GUncertain significance
Select item 2685597	GRCh37/hg19 17p12-11.2(chr17:15694772-20582794)x1	ADORA2B, AKAP10 +61 more	Copy number loss	not provided	GPathogenic
Select item 2684836	GRCh37/hg19 17p12-11.2(chr17:15633208-16567624)x3	ADORA2B, CENPV +10 more	Copy number gain	not provided	GUncertain significance
Select item 2672166	NM_006311.4(NCOR1):c.6332A>C (p.His2111Pro)	NCOR1 (H2008P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2647506	NM_006311.4(NCOR1):c.148G>A (p.Val50Met)	NCOR1 (V50M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2647505	NM_006311.4(NCOR1):c.2568A>G (p.Arg856=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647504	NM_006311.4(NCOR1):c.3242C>T (p.Pro1081Leu)	NCOR1 (P1081L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2633641	NM_006311.4(NCOR1):c.6728C>T (p.Thr2243Met)	NCOR1, TTC19 (T2140M +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GUncertain significance
Select item 2632202	NM_006311.4(NCOR1):c.5831A>T (p.Asp1944Val)	NCOR1 (D1944V)	Single nucleotide variant (missense variant +1 more)	NCOR1-related disorder	GUncertain significance
Select item 2610718	NM_006311.4(NCOR1):c.7202T>C (p.Ile2401Thr)	NCOR1, TTC19 (I2401T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603465	NM_006311.4(NCOR1):c.1744A>G (p.Lys582Glu)	NCOR1 (K473E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600335	NM_006311.4(NCOR1):c.6094C>G (p.Pro2032Ala)	NCOR1 (P2032A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588473	NM_006311.4(NCOR1):c.3671A>G (p.Asn1224Ser)	NCOR1 (N1240S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570308	NM_006311.4(NCOR1):c.5299A>G (p.Met1767Val)	NCOR1 (M1783V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570260	NM_006311.4(NCOR1):c.1838C>T (p.Pro613Leu)	NCOR1 (P504L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557272	NM_006311.4(NCOR1):c.2510A>G (p.Glu837Gly)	NCOR1 (E837G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555745	NM_006311.4(NCOR1):c.5962A>C (p.Lys1988Gln)	NCOR1 (K1988Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553919	NM_006311.4(NCOR1):c.3301A>G (p.Thr1101Ala)	NCOR1 (T1101A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538809	NM_006311.4(NCOR1):c.4724A>G (p.His1575Arg)	NCOR1 (H1575R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533131	NM_006311.4(NCOR1):c.6073T>C (p.Ser2025Pro)	NCOR1 (S1922P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532794	NM_006311.4(NCOR1):c.130C>T (p.Arg44Cys)	NCOR1 (R44C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527894	NM_006311.4(NCOR1):c.2030A>G (p.Asn677Ser)	NCOR1 (N568S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508691	NM_006311.4(NCOR1):c.49C>G (p.Gln17Glu)	NCOR1 (Q17E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495258	NM_006311.4(NCOR1):c.6817G>A (p.Gly2273Arg)	NCOR1, TTC19 (G2170R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490395	NM_006311.4(NCOR1):c.6517G>A (p.Ala2173Thr)	NCOR1 (A2173T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488269	NM_006311.4(NCOR1):c.3640G>A (p.Gly1214Ser)	NCOR1 (G1214S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486241	NM_006311.4(NCOR1):c.3073C>T (p.Pro1025Ser)	NCOR1 (P1041S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481133	NM_006311.4(NCOR1):c.2527G>A (p.Glu843Lys)	NCOR1 (E750K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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