ClinVar for Gene (Select 10771) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3068340	NM_001370100.5(ZMYND11):c.1483C>T (p.Arg495Ter)	LOC126860802, ZMYND11 (R338* +15 more)	Single nucleotide variant (nonsense +1 more)	Intellectual disability, autosomal dominant 30	GPathogenic
Select item 3063160	GRCh37/hg19 10p15.3(chr10:115344-205301)x3	ZMYND11	Copy number gain	not specified	GUncertain significance
Select item 3050113	NM_001370100.5(ZMYND11):c.1741T>C (p.Cys581Arg)	ZMYND11 (C424R +15 more)	Single nucleotide variant (missense variant +1 more)	ZMYND11-related condition	GUncertain significance
Select item 3036673	NM_001370100.5(ZMYND11):c.1080G>C (p.Gly360=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	ZMYND11-related condition	GLikely benign
Select item 3031612	NM_001370100.5(ZMYND11):c.1108C>T (p.Arg370Ter)	ZMYND11 (R213* +14 more)	Single nucleotide variant (nonsense +1 more)	ZMYND11-related condition	GLikely pathogenic
Select item 3024222	NM_001370100.5(ZMYND11):c.788_791del (p.Tyr263fs)	ZMYND11 (Y106fs +13 more)	Deletion (frameshift variant +2 more)	Intellectual disability, autosomal dominant 30	GLikely pathogenic
Select item 2909259	NM_001370100.5(ZMYND11):c.1038C>T (p.Ala346=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2907981	NM_001370100.5(ZMYND11):c.8G>A (p.Arg3His)	ZMYND11 (R3H)	Single nucleotide variant (missense variant +3 more)	not provided	GLikely benign
Select item 2904007	NM_001370100.5(ZMYND11):c.609+8C>T	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2888819	NM_001370100.5(ZMYND11):c.277-4G>A	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881564	NM_001370100.5(ZMYND11):c.595C>G (p.Pro199Ala)	ZMYND11 (P128A +8 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2880578	NM_001370100.5(ZMYND11):c.1501-10_1501-9del	LOC126860802, ZMYND11	Deletion (intron variant)	not provided	GLikely benign
Select item 2880300	NM_001370100.5(ZMYND11):c.439-16C>G	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2879114	NM_001370100.5(ZMYND11):c.630C>T (p.Tyr210=)	ZMYND11	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2877755	NM_001370100.5(ZMYND11):c.609+18T>A	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2877599	NM_001370100.5(ZMYND11):c.546C>G (p.Asp182Glu)	ZMYND11 (D160E +8 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2877178	NM_001370100.5(ZMYND11):c.754-9C>A	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2874534	NM_001370100.5(ZMYND11):c.698-14A>G	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2874086	NM_001370100.5(ZMYND11):c.1227+17G>A	ZMYND11	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2873135	NM_001370100.5(ZMYND11):c.754-13T>G	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2873038	NM_001370100.5(ZMYND11):c.439-16C>T	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869818	NM_001370100.5(ZMYND11):c.1427A>G (p.Asn476Ser)	LOC126860802, ZMYND11 (N319S +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2869728	NM_001370100.5(ZMYND11):c.1500+13G>A	LOC126860802, ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869639	NM_001370100.5(ZMYND11):c.832-18A>G	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869581	NM_001370100.5(ZMYND11):c.697+15_697+16insGGT	ZMYND11	Insertion (intron variant)	not provided	GLikely benign
Select item 2869439	NM_001370100.5(ZMYND11):c.1687-17C>T	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868909	NM_001370100.5(ZMYND11):c.1501-18G>A	LOC126860802, ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868641	NM_001370100.5(ZMYND11):c.1380C>T (p.Asp460=)	LOC126860802, ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2867814	NM_001370100.5(ZMYND11):c.1227+16C>T	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2862741	NM_001370100.5(ZMYND11):c.872_873insA (p.Phe291fs)	ZMYND11 (F236fs +14 more)	Insertion (frameshift variant +1 more)	not provided	GPathogenic
Select item 2854479	NM_001370100.5(ZMYND11):c.1473G>T (p.Glu491Asp)	LOC126860802, ZMYND11 (E372D +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2853691	NM_001370100.5(ZMYND11):c.1080G>A (p.Gly360=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2847530	NM_001370100.5(ZMYND11):c.1377C>G (p.Asn459Lys)	LOC126860802, ZMYND11 (N365K +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2838371	NM_001370100.5(ZMYND11):c.1008C>G (p.His336Gln)	ZMYND11 (H260Q +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2819911	NM_001370100.5(ZMYND11):c.777G>A (p.Lys259=)	ZMYND11	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2807817	NM_001370100.5(ZMYND11):c.999T>G (p.His333Gln)	ZMYND11 (H239Q +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2807434	NM_001370100.5(ZMYND11):c.439-3T>C	ZMYND11	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2806539	NM_001370100.5(ZMYND11):c.136G>A (p.Gly46Ser)	ZMYND11 (G29S +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 2798702	NM_001370100.5(ZMYND11):c.1405G>C (p.Asp469His)	LOC126860802, ZMYND11 (D312H +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2797666	NM_001370100.5(ZMYND11):c.921_950+7dup	ZMYND11	Duplication (splice donor variant)	not provided	GUncertain significance
Select item 2792928	NM_001370100.5(ZMYND11):c.30G>A (p.Ala10=)	ZMYND11	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 2792509	NM_001370100.5(ZMYND11):c.979G>A (p.Asp327Asn)	ZMYND11 (D170N +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2790739	NM_001370100.5(ZMYND11):c.1686+13C>G	LOC126860802, ZMYND11 (L566V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2788168	NM_001370100.5(ZMYND11):c.697+20_697+22dup	ZMYND11	Duplication (intron variant)	not provided	GLikely benign
Select item 2785423	NM_001370100.5(ZMYND11):c.773G>C (p.Cys258Ser)	ZMYND11 (C156S +13 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2784072	NM_001370100.5(ZMYND11):c.1501-16del	LOC126860802, ZMYND11	Deletion (intron variant)	not provided	GLikely benign
Select item 2781826	NM_001370100.5(ZMYND11):c.116+18C>T	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2780500	NM_001370100.5(ZMYND11):c.732A>G (p.Leu244=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2779090	NM_001370100.5(ZMYND11):c.990C>T (p.Val330=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2779072	NM_001370100.5(ZMYND11):c.1158+7G>A	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2770957	NM_001370100.5(ZMYND11):c.967G>C (p.Glu323Gln)	ZMYND11 (E166Q +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2768805	NM_001370100.5(ZMYND11):c.831+15T>C	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2763153	NM_001370100.5(ZMYND11):c.1773C>T (p.His591=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2753572	NM_001370100.5(ZMYND11):c.1640C>T (p.Ala547Val)	LOC126860802, ZMYND11 (A492V +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2752160	NM_001370100.5(ZMYND11):c.831+10A>G	ZMYND11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2730425	NM_001370100.5(ZMYND11):c.1438G>C (p.Asp480His)	LOC126860802, ZMYND11 (D361H +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2720047	NM_001370100.5(ZMYND11):c.358C>T (p.Arg120Cys)	ZMYND11 (R103C +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2716969	NM_001370100.5(ZMYND11):c.698-13_698-8del	ZMYND11	Deletion (intron variant)	not provided	GUncertain significance
Select item 2712367	NM_001370100.5(ZMYND11):c.1047G>A (p.Glu349=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2690462	NM_001370100.5(ZMYND11):c.906A>C (p.Glu302Asp)	ZMYND11 (E145D +14 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2672254	NM_006624.7(ZMYND11):c.-20+114C>A	ZMYND11	Single nucleotide variant (5 prime UTR variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2664693	NM_001370100.5(ZMYND11):c.1678A>C (p.Lys560Gln)	LOC126860802, ZMYND11 (K403Q +15 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2663152	NM_001370100.5(ZMYND11):c.705_708del (p.Glu236fs)	ZMYND11 (E142fs +11 more)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 2640265	NM_001370100.5(ZMYND11):c.1278G>A (p.Thr426=)	LOC126860802, ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2640264	NM_001370100.5(ZMYND11):c.277-2718C>T	ZMYND11	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2581381	NM_001370100.5(ZMYND11):c.1038_1039delinsGG (p.Cys347Gly)	ZMYND11 (C190G +14 more)	Indel (missense variant +1 more)	not specified	GUncertain significance
Select item 2577935	NM_001370100.5(ZMYND11):c.1686+1G>T	LOC126860802, ZMYND11 (V509L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 2577598	NM_001370100.5(ZMYND11):c.1795C>T (p.Arg599Cys)	ZMYND11 (R442C +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 2576855	NM_001370100.5(ZMYND11):c.185A>T (p.Asp62Val)	ZMYND11 (D22V +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2576601	NM_001370100.5(ZMYND11):c.1390_1391insCC (p.Gln464fs)	LOC126860802, ZMYND11 (Q307fs +15 more)	Insertion (frameshift variant +1 more)	Intellectual disability, autosomal dominant 30	GLikely pathogenic
Select item 2575988	NM_001370100.5(ZMYND11):c.1195C>T (p.Arg399Ter)	ZMYND11 (R242* +13 more)	Single nucleotide variant (nonsense +2 more)	not provided	GLikely pathogenic
Select item 2556744	NM_001370100.5(ZMYND11):c.824A>T (p.Tyr275Phe)	ZMYND11 (Y181F +13 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2535434	NM_001370100.5(ZMYND11):c.1158+5G>A	ZMYND11	Single nucleotide variant (intron variant)	Inborn genetic diseases	GUncertain significance
Select item 2532450	NM_001370100.5(ZMYND11):c.1571T>C (p.Met524Thr)	LOC126860802, ZMYND11 (M405T +15 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2505109	NM_001370100.5(ZMYND11):c.185A>G (p.Asp62Gly)	ZMYND11 (D22G +3 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	Gnot provided
Select item 2504781	NM_001370100.5(ZMYND11):c.1073G>C (p.Arg358Pro)	ZMYND11 (R201P +14 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2503414	NM_001370100.5(ZMYND11):c.876_882del (p.Phe293fs)	ZMYND11 (F136fs +14 more)	Microsatellite (frameshift variant +1 more)	not provided	GPathogenic
Select item 2502594	NM_001370100.5(ZMYND11):c.373A>G (p.Lys125Glu)	ZMYND11 (K103E +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2488659	NM_001370100.5(ZMYND11):c.20G>C (p.Arg7Thr)	ZMYND11 (R7T)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2471280	NM_001370100.5(ZMYND11):c.1394G>A (p.Ser465Asn)	LOC126860802, ZMYND11 (S410N +15 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2444205	NM_001370100.5(ZMYND11):c.128G>C (p.Arg43Pro)	ZMYND11 (R21P +3 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2444083	NM_001370100.5(ZMYND11):c.1781A>G (p.His594Arg)	ZMYND11 (H437R +15 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2442370	NM_001370100.5(ZMYND11):c.4G>A (p.Ala2Thr)	ZMYND11 (A2T)	Single nucleotide variant (missense variant +3 more)	Intellectual disability, autosomal dominant 30	GLikely pathogenic
Select item 2438665	NM_001370100.5(ZMYND11):c.64A>G (p.Ile22Val)	ZMYND11 (I22V)	Single nucleotide variant (missense variant +3 more)	not provided +1 more	GUncertain significance
Select item 2438664	NM_001370100.5(ZMYND11):c.812A>G (p.Asn271Ser)	ZMYND11 (N114S +13 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2438663	NM_001370100.5(ZMYND11):c.1000C>T (p.Arg334Trp)	ZMYND11 (R177W +14 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2438662	NM_001370100.5(ZMYND11):c.142C>T (p.His48Tyr)	ZMYND11 (H26Y +3 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2438661	NM_001370100.5(ZMYND11):c.1199G>A (p.Arg400His)	ZMYND11 (R243H +13 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2438659	NM_001370100.5(ZMYND11):c.1370C>T (p.Thr457Ile)	LOC126860802, ZMYND11 (T300I +15 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2430631	NM_001370100.5(ZMYND11):c.1796G>A (p.Arg599His)	ZMYND11 (R442H +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 2430481	NM_001370100.5(ZMYND11):c.254A>C (p.Tyr85Ser)	ZMYND11 (Y45S +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2430310	NM_001370100.5(ZMYND11):c.106C>T (p.Arg36Cys)	ZMYND11 (R36C)	Single nucleotide variant (missense variant +3 more)	See cases	GUncertain significance
Select item 2428927	NM_001370100.5(ZMYND11):c.656A>T (p.Asp219Val)	ZMYND11 (D125V +9 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2425625	NC_000010.10:g.(?_225953)_(298410_?)dup	ZMYND11	Duplication	not provided	GUncertain significance
Select item 2425624	NC_000010.10:g.(?_267115)_(460070_?)dup	DIP2C, ZMYND11	Duplication	not provided	GUncertain significance
Select item 2425623	NC_000010.10:g.(?_267115)_(298410_?)del	ZMYND11	Deletion	not provided	GPathogenic
Select item 2418602	NM_001370100.5(ZMYND11):c.1404T>C (p.His468=)	LOC126860802, ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2418187	NM_001370100.5(ZMYND11):c.1122G>A (p.Glu374=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2413409	NM_001370100.5(ZMYND11):c.1378G>A (p.Asp460Asn)	LOC126860802, ZMYND11 (D303N +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2322461	NM_001370100.5(ZMYND11):c.1375A>C (p.Asn459His)	LOC126860802, ZMYND11 (N302H +15 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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