ClinVar Miner

List of variants in gene MYH14 reported as benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400
NM_001145809.2(MYH14):c.1114+13C>T rs11666328
NM_001145809.2(MYH14):c.1149T>C (p.Phe383=) rs61734424
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044
NM_001145809.2(MYH14):c.1329+15C>T rs200176028
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.2041G>C (p.Gly681Arg) rs75915336
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.2600G>A (p.Arg867His) rs547836952
NM_001145809.2(MYH14):c.2763A>G (p.Lys921=) rs191788683
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.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.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.4255C>T (p.Arg1419Trp) rs115019972
NM_001145809.2(MYH14):c.4586G>A (p.Arg1529His) rs185232438
NM_001145809.2(MYH14):c.4596C>T (p.Ala1532=) rs35453633
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363
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.5083G>C (p.Gly1695Arg) rs199915414
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.5334T>C (p.Gly1778=) rs115844649
NM_001145809.2(MYH14):c.5430G>A (p.Ser1810=) rs3745509
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.5533C>T (p.Arg1845Trp) rs199600574
NM_001145809.2(MYH14):c.5678+12C>T rs3826772
NM_001145809.2(MYH14):c.5683C>T (p.Arg1895Cys) rs200485394
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_001145809.2(MYH14):c.5991G>A (p.Thr1997=) rs181567755
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.660G>T (p.Ser220=) rs201835322
NM_001145809.2(MYH14):c.826A>G (p.Ile276Val) rs55645295
NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr) rs590722

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