ClinVar for Gene (Select 9611) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 196

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 condition	GBenign
Select item 3058498	NM_006311.4(NCOR1):c.6678G>A (p.Met2226Ile)	NCOR1 (M2123I +1 more)	Single nucleotide variant (missense variant)	NCOR1-related condition	GLikely benign
Select item 3056547	NM_006311.4(NCOR1):c.3436C>A (p.Arg1146=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GLikely benign
Select item 3056111	NM_006311.4(NCOR1):c.5986GTT[1] (p.Val1997del)	NCOR1 (V1894del +1 more)	Microsatellite (inframe deletion)	NCOR1-related condition	GBenign
Select item 3055775	NM_006311.4(NCOR1):c.2445C>T (p.Pro815=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GBenign
Select item 3055358	NM_006311.4(NCOR1):c.2366G>C (p.Ser789Thr)	NCOR1 (S696T +2 more)	Single nucleotide variant (missense variant)	NCOR1-related condition	GLikely benign
Select item 3054351	NM_006311.4(NCOR1):c.6010+6T>C	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related condition	GLikely benign
Select item 3052795	NM_006311.4(NCOR1):c.675T>A (p.Pro225=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GBenign
Select item 3052555	NM_006311.4(NCOR1):c.180G>A (p.Gln60=)	NCOR1	Single nucleotide variant (synonymous variant +1 more)	NCOR1-related condition	GBenign
Select item 3050696	NM_006311.4(NCOR1):c.6441C>T (p.Tyr2147=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GBenign
Select item 3049993	NM_006311.4(NCOR1):c.1488G>A (p.Gly496=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GBenign
Select item 3049594	NM_006311.4(NCOR1):c.1352+10A>G	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related condition	GLikely benign
Select item 3049019	NM_006311.4(NCOR1):c.6312A>G (p.Glu2104=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GLikely benign
Select item 3042406	NM_006311.4(NCOR1):c.2250G>A (p.Ala750=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GLikely benign
Select item 3039988	NM_006311.4(NCOR1):c.768T>C (p.Gly256=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GBenign
Select item 3038963	NM_006311.4(NCOR1):c.5076G>A (p.Pro1692=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	GLikely benign
Select item 3038527	NM_006311.4(NCOR1):c.3309C>T (p.Pro1103=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	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 condition	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 condition	GBenign
Select item 3034508	NM_006311.4(NCOR1):c.2058T>C (p.Thr686=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related condition	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 condition	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 condition	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)	NCOR1-related condition +1 more	GConflicting classifications of pathogenicity
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 condition	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 condition	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
Select item 2478170	NM_006311.4(NCOR1):c.6269C>T (p.Ser2090Phe)	NCOR1 (S1987F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468826	NM_006311.4(NCOR1):c.3724A>G (p.Ser1242Gly)	NCOR1 (S1242G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465065	NM_006311.4(NCOR1):c.6209C>T (p.Ser2070Leu)	NCOR1 (S1967L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464395	NM_006311.4(NCOR1):c.1703C>T (p.Thr568Ile)	NCOR1 (T459I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408898	NM_006311.4(NCOR1):c.3064G>A (p.Val1022Ile)	NCOR1 (V1022I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408754	NM_006311.4(NCOR1):c.5939G>A (p.Ser1980Asn)	NCOR1 (S1980N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356539	NM_006311.4(NCOR1):c.6773C>G (p.Ala2258Gly)	NCOR1, TTC19 (A2258G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351621	NM_006311.4(NCOR1):c.5086G>C (p.Ala1696Pro)	NCOR1 (A1712P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348112	NM_006311.4(NCOR1):c.4592C>T (p.Ala1531Val)	NCOR1 (A1531V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340283	NM_006311.4(NCOR1):c.5611C>G (p.Leu1871Val)	NCOR1 (L1871V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336917	NM_006311.4(NCOR1):c.3497C>G (p.Thr1166Ser)	NCOR1 (T1182S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334774	NM_006311.4(NCOR1):c.3128C>T (p.Thr1043Ile)	NCOR1 (T1043I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330638	NM_006311.4(NCOR1):c.3083G>A (p.Arg1028Gln)	NCOR1 (R1044Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328635	NM_006311.4(NCOR1):c.5149G>A (p.Glu1717Lys)	NCOR1 (E1733K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323033	NM_006311.4(NCOR1):c.272C>T (p.Pro91Leu)	NCOR1 (P91L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321851	NM_006311.4(NCOR1):c.739G>A (p.Ala247Thr)	NCOR1 (A138T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316357	NM_006311.4(NCOR1):c.1327C>G (p.His443Asp)	NCOR1 (H443D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311268	NM_006311.4(NCOR1):c.4888G>A (p.Asp1630Asn)	NCOR1 (D1630N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306699	NM_006311.4(NCOR1):c.6939C>A (p.Asp2313Glu)	NCOR1, TTC19 (D2313E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 2