ClinVar Miner

List of variants in gene MYH14 reported as likely benign for Nonsyndromic Hearing Loss, Dominant

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_001145809.2(MYH14):c.*122A>C rs12978083
NM_001145809.2(MYH14):c.*301C>T rs529409417
NM_001145809.2(MYH14):c.*302G>A rs544178350
NM_001145809.2(MYH14):c.*389C>G rs149455351
NM_001145809.2(MYH14):c.-13C>T rs187670753
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817
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.1483-10G>A rs73061136
NM_001145809.2(MYH14):c.1755C>T (p.Gly585=) rs61731838
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.2205C>G (p.Arg735=) rs378811
NM_001145809.2(MYH14):c.2359G>A (p.Glu787Lys) rs397516628
NM_001145809.2(MYH14):c.2600G>A (p.Arg867His) rs547836952
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.3079C>T (p.Leu1027=) rs113152264
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.3468-3C>T rs78192108
NM_001145809.2(MYH14):c.3663C>T (p.Asn1221=) rs78573213
NM_001145809.2(MYH14):c.3680+9C>T rs76579307
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn) rs202225655
NM_001145809.2(MYH14):c.4138-13C>T rs183327883
NM_001145809.2(MYH14):c.4596C>T (p.Ala1532=) rs35453633
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.483G>A (p.Met161Ile) rs34773557
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.5466G>A (p.Leu1822=) rs10419343
NM_001145809.2(MYH14):c.5529C>T (p.Ser1843=) rs12610591
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_001145809.2(MYH14):c.6012A>T (p.Leu2004=) rs73932457
NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr) rs590722

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