ClinVar Miner

List of variants in gene MYH14 reported by PreventionGenetics

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Gene type:
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Total variants: 31
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HGVS dbSNP
NM_001145809.2(MYH14):c.1114+13C>T rs11666328
NM_001145809.2(MYH14):c.1149T>C (p.Phe383=) rs61734424
NM_001145809.2(MYH14):c.1155C>T (p.Asn385=) rs558991834
NM_001145809.2(MYH14):c.1483-10G>A rs73061136
NM_001145809.2(MYH14):c.1755C>T (p.Gly585=) rs61731838
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.2250A>G (p.Pro750=) rs1651553
NM_001145809.2(MYH14):c.2355-14C>T rs12981413
NM_001145809.2(MYH14):c.2355-17C>T rs28482851
NM_001145809.2(MYH14):c.2827-9A>C rs3745503
NM_001145809.2(MYH14):c.3018G>A (p.Leu1006=) rs3745504
NM_001145809.2(MYH14):c.3033+11T>C rs930086
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.3468-3C>T rs78192108
NM_001145809.2(MYH14):c.3680+9C>T rs76579307
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.4752+15C>T rs745696035
NM_001145809.2(MYH14):c.4752+16G>A rs10406788
NM_001145809.2(MYH14):c.4753-9C>T rs45591233
NM_001145809.2(MYH14):c.5128-11G>A rs774151356
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_001145809.2(MYH14):c.5281C>A (p.Arg1761=) rs116035034
NM_001145809.2(MYH14):c.5430G>A (p.Ser1810=) rs3745509
NM_001145809.2(MYH14):c.5469+16C>T rs3745510
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073
NM_001145809.2(MYH14):c.5678+12C>T rs3826772
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_001145809.2(MYH14):c.657G>A (p.Ala219=) rs4801822
NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr) rs590722

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