ClinVar Miner

List of variants in gene MYH14 reported as benign for Autosomal dominant nonsyndromic hearing loss 4A

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.3033+11T>C rs930086 0.86981
NM_001145809.2(MYH14):c.*216T>G rs627491 0.86114
NM_001145809.2(MYH14):c.5788-41A>G rs889002 0.83244
NM_001145809.2(MYH14):c.5678+12C>T rs3826772 0.78229
NM_001145809.2(MYH14):c.2694+30T>C rs1529492 0.74599
NM_001145809.2(MYH14):c.2250A>G (p.Pro750=) rs1651553 0.74436
NM_001145809.2(MYH14):c.5469+16C>T rs3745510 0.64922
NM_001145809.2(MYH14):c.5430G>A (p.Ser1810=) rs3745509 0.63924
NM_001145809.2(MYH14):c.657G>A (p.Ala219=) rs4801822 0.56915
NM_001145809.2(MYH14):c.3018G>A (p.Leu1006=) rs3745504 0.53291
NM_001145809.2(MYH14):c.3681-26A>T rs788337 0.50766
NM_001145809.2(MYH14):c.2355-14C>T rs12981413 0.46235
NM_001145809.2(MYH14):c.2205C>G (p.Arg735=) rs378811 0.38312
NM_001145809.2(MYH14):c.*122A>C rs12978083 0.33223
NM_001145809.2(MYH14):c.1114+13C>T rs11666328 0.32285
NM_001145809.2(MYH14):c.2355-17C>T rs28482851 0.23202
NM_001145809.2(MYH14):c.3680+9C>T rs76579307 0.20534
NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr) rs590722 0.14959
NM_001145809.2(MYH14):c.2827-9A>C rs3745503 0.14515
NM_001145809.2(MYH14):c.1483-10G>A rs73061136 0.09105
NM_001145809.2(MYH14):c.1755C>T (p.Gly585=) rs61731838 0.07411
NM_001145809.2(MYH14):c.1149T>C (p.Phe383=) rs61734424 0.06194
NM_001145809.2(MYH14):c.1890C>T (p.Val630=) rs77895476 0.03277
NM_001145809.2(MYH14):c.474T>C (p.Ile158=) rs34796700 0.02809
NM_001145809.2(MYH14):c.5281C>A (p.Arg1761=) rs116035034 0.02785
NM_001145809.2(MYH14):c.4753-9C>T rs45591233 0.02396
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191 0.01884
NM_001145809.2(MYH14):c.3468-3C>T rs78192108 0.01724
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817 0.01645
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557 0.01615
NM_001145809.2(MYH14):c.4596C>T (p.Ala1532=) rs35453633 0.01258
NM_001145809.2(MYH14):c.6012A>T (p.Leu2004=) rs73932457 0.01253
NM_001145809.2(MYH14):c.4741G>A (p.Val1581Ile) rs680446 0.01091
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081 0.01050
NM_001145809.2(MYH14):c.5466G>A (p.Leu1822=) rs10419343 0.01020
NM_001145809.2(MYH14):c.5334T>C (p.Gly1778=) rs115844649 0.00878
NM_001145809.2(MYH14):c.3663C>T (p.Asn1221=) rs78573213 0.00779
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624 0.00710
NM_001145809.2(MYH14):c.2792G>A (p.Arg931His) rs200351672 0.00460
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400 0.00249
NM_001145809.2(MYH14):c.5529C>T (p.Ser1843=) rs12610591 0.00248
NM_001145809.2(MYH14):c.*389C>G rs149455351 0.00223
NM_001145809.2(MYH14):c.3079C>T (p.Leu1027=) rs113152264 0.00210
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363 0.00158
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006 0.00071
NM_001145809.2(MYH14):c.-13C>T rs187670753 0.00057
NM_001145809.2(MYH14):c.4753-5A>G rs118097099 0.00036
NM_001145809.2(MYH14):c.1133C>T (p.Ser378Leu) rs150806988 0.00011
NM_001145809.2(MYH14):c.2600G>A (p.Arg867His) rs547836952 0.00008
NM_001145809.2(MYH14):c.*302G>A rs544178350 0.00004
NM_001145809.2(MYH14):c.2359G>A (p.Glu787Lys) rs397516628 0.00002
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044 0.00001
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196

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