"NCOR2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

Search results

Items: 99

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039817	NM_006312.6(NCOR2):c.7410G>A (p.Ala2470=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 2628878	NM_006312.6(NCOR2):c.7400G>A (p.Arg2467Gln)	NCOR2 (R2411Q +2 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GUncertain significance
Select item 3052029	NM_006312.6(NCOR2):c.7364-5C>T	NCOR2	Single nucleotide variant (intron variant)	NCOR2-related condition	GLikely benign
Select item 3047964	NM_006312.6(NCOR2):c.7359C>T (p.Ser2453=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3050430	NM_006312.6(NCOR2):c.7296G>A (p.Ser2432=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3050726	NM_006312.6(NCOR2):c.7263G>T (p.Gly2421=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3044033	NM_006312.6(NCOR2):c.7189G>A (p.Gly2397Ser)	NCOR2 (G2341S +2 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GLikely benign
Select item 3044510	NM_006312.6(NCOR2):c.7188C>T (p.Gly2396=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 2643548	NM_006312.6(NCOR2):c.6720G>A (p.Pro2240=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition +1 more	GLikely benign
Select item 3039576	NM_006312.6(NCOR2):c.6699C>T (p.His2233=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3041930	NM_006312.6(NCOR2):c.6675G>A (p.Pro2225=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3041995	NM_006312.6(NCOR2):c.6625A>C (p.Thr2209Pro)	NCOR2 (T2199P +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3033094	NM_006312.6(NCOR2):c.6591C>T (p.Ser2197=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3033778	NM_006312.6(NCOR2):c.6573C>G (p.Ala2191=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3034934	NM_006312.6(NCOR2):c.6411+8C>T	NCOR2	Single nucleotide variant (intron variant)	NCOR2-related condition	GLikely benign
Select item 3034040	NM_006312.6(NCOR2):c.6345G>A (p.Pro2115=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3045095	NM_006312.6(NCOR2):c.6251G>A (p.Arg2084Gln)	NCOR2 (R2074Q +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GLikely benign
Select item 3050628	NM_006312.6(NCOR2):c.6156C>T (p.Pro2052=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3041055	NM_006312.6(NCOR2):c.6041C>T (p.Ser2014Leu)	NCOR2 (S2004L +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GLikely benign
Select item 3039820	NM_006312.6(NCOR2):c.6030G>A (p.Ala2010=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3049665	NM_006312.6(NCOR2):c.6011C>T (p.Ala2004Val)	NCOR2 (A1994V +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3056105	NM_006312.6(NCOR2):c.6001C>T (p.Pro2001Ser)	NCOR2 (P1991S +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3055423	NM_006312.6(NCOR2):c.5998G>A (p.Ala2000Thr)	NCOR2 (A1990T +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3038759	NM_006312.6(NCOR2):c.5931G>T (p.Glu1977Asp)	NCOR2 (E1967D +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3049982	NM_006312.6(NCOR2):c.5928G>A (p.Ser1976=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3034760	NM_006312.6(NCOR2):c.5892C>T (p.Ser1964=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3045455	NM_006312.6(NCOR2):c.5796C>T (p.Pro1932=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3055510	NM_006312.6(NCOR2):c.5748C>T (p.Cys1916=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 1301427	NM_006312.6(NCOR2):c.5718G>A (p.Pro1906=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition +1 more	GBenign
Select item 3043941	NM_006312.6(NCOR2):c.5709C>T (p.Pro1903=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3060014	NM_006312.6(NCOR2):c.5500AGCAGCGGC[3] (p.Gly1839_Gly1840insSerSerGly)	NCOR2	Microsatellite (inframe insertion)	NCOR2-related condition	GBenign
Select item 3040147	NM_006312.6(NCOR2):c.5379G>A (p.Ser1793=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3048655	NM_006312.6(NCOR2):c.5148C>T (p.Arg1716=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 1278544	NM_006312.6(NCOR2):c.5095G>A (p.Ala1699Thr)	NCOR2 (A1689T +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition +1 more	GBenign
Select item 3041788	NM_006312.6(NCOR2):c.5034G>A (p.Ala1678=)	NCOR2	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 3059345	NM_006312.6(NCOR2):c.4959A>G (p.Arg1653=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 2643551	NM_006312.6(NCOR2):c.4936+7G>T	NCOR2	Single nucleotide variant (intron variant)	NCOR2-related condition +1 more	GLikely benign
Select item 3040896	NM_006312.6(NCOR2):c.4893C>T (p.Ala1631=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3033783	NM_006312.6(NCOR2):c.4803C>T (p.Pro1601=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3034206	NM_006312.6(NCOR2):c.4776C>T (p.Ile1592=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3052786	NM_006312.6(NCOR2):c.4758G>A (p.Thr1586=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 2643552	NM_006312.6(NCOR2):c.4701G>A (p.Pro1567=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition +1 more	GLikely benign
Select item 3060500	NM_006312.6(NCOR2):c.4623G>A (p.Leu1541=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3060007	NM_006312.6(NCOR2):c.4602T>C (p.Gly1534=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 2634689	NM_006312.6(NCOR2):c.4576G>A (p.Ala1526Thr)	NCOR2 (A1516T +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition +1 more	GUncertain significance
Select item 3038090	NM_006312.6(NCOR2):c.4552T>A (p.Ser1518Thr)	NCOR2 (S1508T +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3042547	NM_006312.6(NCOR2):c.4458C>T (p.Pro1486=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3043001	NM_006312.6(NCOR2):c.4389G>A (p.Ala1463=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3039792	NM_006312.6(NCOR2):c.4383C>T (p.Thr1461=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3037917	NM_006312.6(NCOR2):c.4383C>G (p.Thr1461=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3055703	NM_006312.6(NCOR2):c.4368G>A (p.Pro1456=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3047009	NM_006312.6(NCOR2):c.4227G>A (p.Pro1409=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition +1 more	GLikely benign
Select item 2643558	NM_006312.6(NCOR2):c.4055G>A (p.Arg1352His)	NCOR2 (R1342H +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition +1 more	GLikely benign
Select item 3058550	NM_006312.6(NCOR2):c.3912G>A (p.Thr1304=)	LOC124849275, NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3049101	NM_006312.6(NCOR2):c.3911C>T (p.Thr1304Met)	LOC124849275, NCOR2 (T1294M +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3058757	NM_006312.6(NCOR2):c.3756G>A (p.Pro1252=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3049938	NM_006312.6(NCOR2):c.3741C>T (p.Ile1247=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3044955	NM_006312.6(NCOR2):c.3612G>A (p.Pro1204=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3058293	NM_006312.6(NCOR2):c.3576G>A (p.Ala1192=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3042889	NM_006312.6(NCOR2):c.3453G>T (p.Gly1151=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3038050	NM_006312.6(NCOR2):c.3282C>T (p.Pro1094=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3041232	NM_006312.6(NCOR2):c.3242-9G>A	NCOR2	Single nucleotide variant (intron variant)	NCOR2-related condition	GBenign
Select item 3044546	NM_006312.6(NCOR2):c.3153C>T (p.Ser1051=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3056908	NM_006312.6(NCOR2):c.3111C>T (p.Ala1037=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3044167	NM_006312.6(NCOR2):c.3078G>A (p.Pro1026=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3055856	NM_006312.6(NCOR2):c.2984C>G (p.Ala995Gly)	NCOR2 (A977G +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 2643559	NM_006312.6(NCOR2):c.2928C>T (p.Ile976=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition +1 more	GLikely benign
Select item 3042831	NM_006312.6(NCOR2):c.2796C>T (p.Gly932=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3059724	NM_006312.6(NCOR2):c.2757T>C (p.Ala919=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3060147	NM_006312.6(NCOR2):c.2715A>T (p.Thr905=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3042754	NM_006312.6(NCOR2):c.2610C>T (p.Ala870=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3041968	NM_006312.6(NCOR2):c.2574C>T (p.Ala858=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3058956	NM_006312.6(NCOR2):c.2342G>A (p.Gly781Glu)	NCOR2 (G763E +1 more)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3058166	NM_006312.6(NCOR2):c.2274C>T (p.Ala758=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3042348	NM_006312.6(NCOR2):c.2250C>T (p.Ser750=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3040309	NM_006312.6(NCOR2):c.2172A>G (p.Leu724=)	NCOR2	Single nucleotide variant (synonymous variant +1 more)	NCOR2-related condition	GLikely benign
Select item 3052384	NM_006312.6(NCOR2):c.1986C>T (p.Leu662=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3043309	NM_006312.6(NCOR2):c.1911C>T (p.Ile637=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3055772	NM_006312.6(NCOR2):c.1611G>A (p.Glu537=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3060828	NM_006312.6(NCOR2):c.1496AGC[14] (p.Gln510_Pro511insGlnGln)	NCOR2	Microsatellite (inframe insertion)	NCOR2-related condition	GBenign
Select item 3055805	NM_006312.6(NCOR2):c.1496AGC[16] (p.Gln510_Pro511insGlnGlnGlnGln)	NCOR2	Microsatellite (inframe insertion)	NCOR2-related condition	GBenign
Select item 3037907	NM_006312.6(NCOR2):c.1496AGC[15] (p.Gln510_Pro511insGlnGlnGln)	NCOR2	Microsatellite (inframe insertion)	NCOR2-related condition	GBenign
Select item 1181246	NM_006312.6(NCOR2):c.1496AGC[13] (p.Gln510dup)	NCOR2	Microsatellite (inframe_insertion)	NCOR2-related condition +2 more	GBenign
Select item 3059003	NM_006312.6(NCOR2):c.1496AGC[9] (p.Gln508_Gln510del)	NCOR2	Microsatellite (inframe deletion)	NCOR2-related condition	GBenign
Select item 3045071	NM_006312.6(NCOR2):c.1497G>A (p.Gln499=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3044605	NM_006312.6(NCOR2):c.1483-9dup	NCOR2	Duplication (intron variant)	NCOR2-related condition	GLikely benign
Select item 3044815	NM_006312.6(NCOR2):c.1414C>T (p.Leu472=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3033831	NM_006312.6(NCOR2):c.1371C>T (p.Phe457=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3060702	NM_006312.6(NCOR2):c.1329-4G>A	NCOR2	Single nucleotide variant (intron variant)	NCOR2-related condition	GBenign
Select item 2643563	NM_006312.6(NCOR2):c.843C>T (p.Ile281=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition +1 more	GLikely benign
Select item 3053222	NM_006312.6(NCOR2):c.723A>C (p.Ala241=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 1286492	NM_006312.6(NCOR2):c.462G>A (p.Pro154=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition +1 more	GBenign
Select item 3052008	NM_006312.6(NCOR2):c.390G>C (p.Ala130=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 3038066	NM_006312.6(NCOR2):c.313A>G (p.Ser105Gly)	NCOR2 (S105G)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3041399	NM_006312.6(NCOR2):c.222C>T (p.Pro74=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GLikely benign
Select item 2643565	NM_006312.6(NCOR2):c.198C>T (p.Pro66=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition +1 more	GLikely benign
Select item 3035234	NM_006312.6(NCOR2):c.155A>G (p.His52Arg)	NCOR2 (H52R)	Single nucleotide variant (missense variant)	NCOR2-related condition	GBenign
Select item 3059626	NM_006312.6(NCOR2):c.9A>C (p.Gly3=)	NCOR2	Single nucleotide variant (synonymous variant)	NCOR2-related condition	GBenign
Select item 3039906	NM_006312.6(NCOR2):c.-6A>C	NCOR2	Single nucleotide variant (5 prime UTR variant)	NCOR2-related condition	GLikely benign

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Items: 99