ClinVar Miner

List of variants in gene MYH14 studied for Nonsyndromic Hearing Loss, Dominant

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Total variants: 121
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HGVS dbSNP
NM_001145809.2(MYH14):c.*122A>C rs12978083
NM_001145809.2(MYH14):c.*142C>G rs770209944
NM_001145809.2(MYH14):c.*144C>T rs773312540
NM_001145809.2(MYH14):c.*216T>G rs627491
NM_001145809.2(MYH14):c.*243G>A rs561898739
NM_001145809.2(MYH14):c.*301C>T rs529409417
NM_001145809.2(MYH14):c.*302G>A rs544178350
NM_001145809.2(MYH14):c.*337C>T rs753307318
NM_001145809.2(MYH14):c.*382_*383TC[12] rs376379600
NM_001145809.2(MYH14):c.*382_*383TC[9] rs376379600
NM_001145809.2(MYH14):c.*389C>G rs149455351
NM_001145809.2(MYH14):c.*400T>C rs886054596
NM_001145809.2(MYH14):c.*474A>G rs886054597
NM_001145809.2(MYH14):c.*531C>T rs886054598
NM_001145809.2(MYH14):c.*64G>A rs779130953
NM_001145809.2(MYH14):c.*667G>A rs886054599
NM_001145809.2(MYH14):c.*81A>G rs772326631
NM_001145809.2(MYH14):c.-13C>T rs187670753
NM_001145809.2(MYH14):c.-3-6C>T rs886054586
NM_001145809.2(MYH14):c.-37C>T rs549250648
NM_001145809.2(MYH14):c.-4+8C>A rs778355560
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817
NM_001145809.2(MYH14):c.1026G>A (p.Pro342=) rs368124508
NM_001145809.2(MYH14):c.1114+13C>G rs11666328
NM_001145809.2(MYH14):c.1114+13C>T rs11666328
NM_001145809.2(MYH14):c.1149T>C (p.Phe383=) rs61734424
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044
NM_001145809.2(MYH14):c.1295G>A (p.Arg432Gln) rs751011647
NM_001145809.2(MYH14):c.1419C>T (p.Arg473=) rs371946306
NM_001145809.2(MYH14):c.1483-10G>A rs73061136
NM_001145809.2(MYH14):c.1755C>T (p.Gly585=) rs61731838
NM_001145809.2(MYH14):c.1779G>A (p.Pro593=) rs557237074
NM_001145809.2(MYH14):c.1800C>T (p.Ala600=) rs745625855
NM_001145809.2(MYH14):c.1890C>T (p.Val630=) rs77895476
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.2068C>G (p.Gln690Glu) rs370124751
NM_001145809.2(MYH14):c.2086G>A (p.Asp696Asn) rs539256005
NM_001145809.2(MYH14):c.2089G>A (p.Gly697Ser) rs778416774
NM_001145809.2(MYH14):c.2126G>A (p.Arg709Gln) rs766802012
NM_001145809.2(MYH14):c.2205C>G (p.Arg735=) rs378811
NM_001145809.2(MYH14):c.2233-13C>A rs368249273
NM_001145809.2(MYH14):c.2250A>G (p.Pro750=) rs1651553
NM_001145809.2(MYH14):c.2271T>C (p.Leu757=) rs371266692
NM_001145809.2(MYH14):c.2279A>G (p.Asn760Ser) rs886054589
NM_001145809.2(MYH14):c.2334C>A (p.Leu778=) rs190941610
NM_001145809.2(MYH14):c.2355-14C>T rs12981413
NM_001145809.2(MYH14):c.2359G>A (p.Glu787Lys) rs397516628
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011
NM_001145809.2(MYH14):c.2487G>A (p.Arg829=) rs746813925
NM_001145809.2(MYH14):c.2600G>A (p.Arg867His) rs547836952
NM_001145809.2(MYH14):c.2748C>T (p.Ala916=) rs886054590
NM_001145809.2(MYH14):c.2792G>A (p.Arg931His) rs200351672
NM_001145809.2(MYH14):c.2827-9A>C rs3745503
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081
NM_001145809.2(MYH14):c.2864G>A (p.Arg955Gln) rs576611342
NM_001145809.2(MYH14):c.2941G>A (p.Val981Met) rs886054591
NM_001145809.2(MYH14):c.3018G>A (p.Leu1006=) rs3745504
NM_001145809.2(MYH14):c.3033+11T>C rs930086
NM_001145809.2(MYH14):c.3079C>T (p.Leu1027=) rs113152264
NM_001145809.2(MYH14):c.3098C>T (p.Thr1033Met) rs201746408
NM_001145809.2(MYH14):c.3141C>T (p.Leu1047=) rs886054592
NM_001145809.2(MYH14):c.3172-12T>C rs374486787
NM_001145809.2(MYH14):c.3207C>G (p.Phe1069Leu) rs886054593
NM_001145809.2(MYH14):c.3259C>T (p.Arg1087Trp) rs368372273
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.3427C>T (p.Leu1143=) rs770366755
NM_001145809.2(MYH14):c.3468-3C>T rs78192108
NM_001145809.2(MYH14):c.3593A>T (p.Gln1198Leu) rs755161446
NM_001145809.2(MYH14):c.3663C>T (p.Asn1221=) rs78573213
NM_001145809.2(MYH14):c.3680+9C>T rs76579307
NM_001145809.2(MYH14):c.36G>A (p.Lys12=) rs372741317
NM_001145809.2(MYH14):c.3704C>T (p.Thr1235Met) rs200988515
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191
NM_001145809.2(MYH14):c.3778G>A (p.Gly1260Ser) rs200272339
NM_001145809.2(MYH14):c.3819C>T (p.Ala1273=) rs750779364
NM_001145809.2(MYH14):c.3850C>T (p.Arg1284Trp) rs201515738
NM_001145809.2(MYH14):c.3871G>T (p.Val1291Leu) rs202242879
NM_001145809.2(MYH14):c.3913C>T (p.Arg1305Cys) rs755704452
NM_001145809.2(MYH14):c.3945G>A (p.Leu1315=) rs769999356
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn) rs202225655
NM_001145809.2(MYH14):c.4138-13C>T rs183327883
NM_001145809.2(MYH14):c.4220G>A (p.Arg1407His) rs553162373
NM_001145809.2(MYH14):c.4296C>T (p.Ser1432=) rs370811348
NM_001145809.2(MYH14):c.440C>T (p.Pro147Leu) rs886054587
NM_001145809.2(MYH14):c.4539+10C>T rs561531825
NM_001145809.2(MYH14):c.4596C>T (p.Ala1532=) rs35453633
NM_001145809.2(MYH14):c.4610G>A (p.Arg1537Gln) rs752388019
NM_001145809.2(MYH14):c.4681G>A (p.Glu1561Lys) rs761025607
NM_001145809.2(MYH14):c.4693C>A (p.Arg1565=) rs769989306
NM_001145809.2(MYH14):c.4731C>T (p.Ser1577=) rs766728732
NM_001145809.2(MYH14):c.4741G>A (p.Val1581Ile) rs680446
NM_001145809.2(MYH14):c.474T>C (p.Ile158=) rs34796700
NM_001145809.2(MYH14):c.4753-5A>G rs118097099
NM_001145809.2(MYH14):c.4753-9C>T rs45591233
NM_001145809.2(MYH14):c.4773C>T (p.Ala1591=) rs746906367
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557
NM_001145809.2(MYH14):c.5041G>A (p.Glu1681Lys) rs556548077
NM_001145809.2(MYH14):c.5127+12C>T rs373755483
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr) rs138001307
NM_001145809.2(MYH14):c.5281C>A (p.Arg1761=) rs116035034
NM_001145809.2(MYH14):c.5334T>C (p.Gly1778=) rs115844649
NM_001145809.2(MYH14):c.535G>A (p.Glu179Lys) rs886054588
NM_001145809.2(MYH14):c.5430G>A (p.Ser1810=) rs3745509
NM_001145809.2(MYH14):c.543C>T (p.Ala181=) rs746669662
NM_001145809.2(MYH14):c.5447G>A (p.Arg1816His) rs201923258
NM_001145809.2(MYH14):c.5466G>A (p.Leu1822=) rs10419343
NM_001145809.2(MYH14):c.5529C>T (p.Ser1843=) rs12610591
NM_001145809.2(MYH14):c.5599C>T (p.Arg1867Cys) rs187789045
NM_001145809.2(MYH14):c.565C>T (p.Arg189Cys) rs200818171
NM_001145809.2(MYH14):c.5678+12C>T rs3826772
NM_001145809.2(MYH14):c.5802C>A (p.Asn1934Lys) rs745991888
NM_001145809.2(MYH14):c.5858G>A (p.Arg1953Gln) rs754203387
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_001145809.2(MYH14):c.5961-10C>T rs776693090
NM_001145809.2(MYH14):c.5990C>T (p.Thr1997Met) rs201986144
NM_001145809.2(MYH14):c.5C>T (p.Ala2Val) rs750407725
NM_001145809.2(MYH14):c.6012A>T (p.Leu2004=) rs73932457
NM_001145809.2(MYH14):c.657G>A (p.Ala219=) rs4801822
NM_001145809.2(MYH14):c.866T>C (p.Ile289Thr) rs777836668
NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr) rs590722

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