ClinVar for Gene (Select 10771) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3375350	NM_001370100.5(ZMYND11):c.517-11C>T	ZMYND11	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3373641	NM_001370100.5(ZMYND11):c.359G>A (p.Arg120His)	ZMYND11 (R103H +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3373525	NM_001370100.5(ZMYND11):c.1252G>T (p.Val418Leu)	LOC126860802, ZMYND11 (V261L +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3373477	NM_001370100.5(ZMYND11):c.300C>G (p.Asp100Glu)	ZMYND11 (D100E +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3371377	NM_001370100.5(ZMYND11):c.739G>T (p.Asp247Tyr)	ZMYND11 (D153Y +11 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3370545	NM_001370100.5(ZMYND11):c.1296A>C (p.Glu432Asp)	LOC126860802, ZMYND11 (E275D +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3369996	NM_001370100.5(ZMYND11):c.912_915del (p.Asn304fs)	ZMYND11 (N147fs +14 more)	Deletion (frameshift variant +1 more)	See cases +1 more	GPathogenic
Select item 3368351	NM_001370100.5(ZMYND11):c.799G>T (p.Ala267Ser)	ZMYND11 (A110S +13 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3368228	NM_001370100.5(ZMYND11):c.482A>C (p.Tyr161Ser)	ZMYND11 (Y107S +8 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3366071	NM_001370100.5(ZMYND11):c.1331G>A (p.Ser444Asn)	LOC126860802, ZMYND11 (S287N +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3362053	NM_001370100.5(ZMYND11):c.1768T>C (p.Trp590Arg)	ZMYND11 (W433R +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 3361615	NM_001370100.5(ZMYND11):c.715G>A (p.Asp239Asn)	ZMYND11 (D145N +11 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3355948	NM_001370100.5(ZMYND11):c.1604G>A (p.Cys535Tyr)	LOC126860802, ZMYND11 (C378Y +15 more)	Single nucleotide variant (missense variant +1 more)	ZMYND11-related disorder	GUncertain significance
Select item 3347530	NM_001370100.5(ZMYND11):c.613del (p.Lys204_Val205insTer)	ZMYND11	Deletion (nonsense +2 more)	ZMYND11-related disorder	GLikely pathogenic
Select item 3346207	NM_001370100.5(ZMYND11):c.1597G>T (p.Glu533Ter)	LOC126860802, ZMYND11 (E376* +15 more)	Single nucleotide variant (nonsense +1 more)	ZMYND11-related disorder	GLikely pathogenic
Select item 3343207	NM_212479.3(ZMYND11):c.-125G>A	ZMYND11	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 3340649	NM_001370100.5(ZMYND11):c.927CTT[1] (p.Phe311del)	ZMYND11 (F154del +14 more)	Microsatellite (inframe_deletion +1 more)	not provided	GLikely pathogenic
Select item 3340629	NM_001370100.5(ZMYND11):c.946C>T (p.Gln316Ter)	ZMYND11 (Q159* +14 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 3338583	NM_001370100.5(ZMYND11):c.573G>C (p.Leu191=)	ZMYND11	Single nucleotide variant (synonymous variant +2 more)	not provided	GUncertain significance
Select item 3334834	NM_001370100.5(ZMYND11):c.697+2T>A	ZMYND11	Single nucleotide variant (splice donor variant +1 more)	Inborn genetic diseases	GLikely pathogenic
Select item 3334833	NM_001370100.5(ZMYND11):c.858_883dup (p.Pro295delinsLeuLysTer)	ZMYND11	Duplication (nonsense +1 more)	Inborn genetic diseases	GPathogenic
Select item 3334832	NM_001370100.5(ZMYND11):c.727_747dup (p.Cys249_His250insMetLeuTyrLysAspThrCys)	ZMYND11	Duplication (inframe_insertion +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3334831	NM_001370100.5(ZMYND11):c.167T>C (p.Leu56Pro)	ZMYND11 (L16P +3 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3257099	NM_001370100.5(ZMYND11):c.150A>G (p.Lys50=)	ZMYND11	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3254942	NM_001370100.5(ZMYND11):c.1381G>A (p.Gly461Ser)	LOC126860802, ZMYND11 (G304S +15 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 3253525	NM_001370100.5(ZMYND11):c.20G>T (p.Arg7Ile)	ZMYND11 (R7I)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3244988	NC_000010.10:g.(?_225953)_(285485_?)dup	ZMYND11	Duplication	not provided	GUncertain significance
Select item 3244987	NC_000010.10:g.(?_225953)_(282875_?)dup	ZMYND11	Duplication	not provided	GUncertain significance
Select item 3244986	NC_000010.10:g.(?_298268)_(298410_?)dup	ZMYND11	Duplication	not provided	GUncertain significance
Select item 3244985	NC_000010.10:g.(?_225953)_(735518_?)dup	DIP2C, ZMYND11	Duplication	not provided	GUncertain significance
Select item 3244984	NC_000010.10:g.(?_282758)_(286930_?)del	ZMYND11	Deletion	not provided	GPathogenic
Select item 3239581	NM_001370100.5(ZMYND11):c.183A>G (p.Lys61=)	ZMYND11	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3234936	NM_001370100.5(ZMYND11):c.1366C>T (p.Gln456Ter)	LOC126860802, ZMYND11 (Q299* +15 more)	Single nucleotide variant (nonsense +1 more)	Intellectual disability, autosomal dominant 30	GLikely pathogenic
Select item 3233320	NM_001370100.5(ZMYND11):c.1073G>A (p.Arg358Gln)	ZMYND11 (R201Q +14 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 3233318	NM_001370100.5(ZMYND11):c.521T>C (p.Ile174Thr)	ZMYND11 (I103T +8 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 3233313	NM_001370100.5(ZMYND11):c.950G>A (p.Arg317Lys)	ZMYND11 (R160K +14 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 1	GUncertain significance
Select item 3193836	NM_001370100.5(ZMYND11):c.922G>A (p.Val308Ile)	ZMYND11 (V206I +14 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3193835	NM_001370100.5(ZMYND11):c.595C>T (p.Pro199Ser)	ZMYND11 (P128S +8 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3193834	NM_001370100.5(ZMYND11):c.438+5G>C	ZMYND11	Single nucleotide variant (intron variant)	Inborn genetic diseases	GLikely pathogenic
Select item 3148908	GRCh37/hg19 10p15.3(chr10:100048-1247374)x1	ADARB2, DIP2C +6 more	Copy number loss	See cases	GPathogenic
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 disorder	GUncertain significance
Select item 3036673	NM_001370100.5(ZMYND11):c.1080G>C (p.Gly360=)	ZMYND11	Single nucleotide variant (synonymous variant +1 more)	ZMYND11-related disorder	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 disorder	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

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