ClinVar Miner

List of variants in gene MYH14 reported as benign

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Gene type:
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Total variants: 60
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HGVS dbSNP
NM_001077186.1(MYH14):c.3369-3C>T rs78192108
NM_001145809.1(MYH14):c.1114+13C>T rs11666328
NM_001145809.1(MYH14):c.1149T>C (p.Phe383=) rs61734424
NM_001145809.1(MYH14):c.1329+15C>T rs200176028
NM_001145809.1(MYH14):c.1483-10G>A rs73061136
NM_001145809.1(MYH14):c.1755C>T (p.Gly585=) rs61731838
NM_001145809.1(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.1(MYH14):c.2041G>C (p.Gly681Arg) rs75915336
NM_001145809.1(MYH14):c.2205C>G (p.Arg735=) rs378811
NM_001145809.1(MYH14):c.2250A>G (p.Pro750=) rs1651553
NM_001145809.1(MYH14):c.2355-14C>T rs12981413
NM_001145809.1(MYH14):c.2355-17C>T rs28482851
NM_001145809.1(MYH14):c.2763A>G (p.Lys921=) rs191788683
NM_001145809.1(MYH14):c.2792G>A (p.Arg931His) rs200351672
NM_001145809.1(MYH14):c.2827-9A>C rs3745503
NM_001145809.1(MYH14):c.3018G>A (p.Leu1006=) rs3745504
NM_001145809.1(MYH14):c.3033+11T>C rs930086
NM_001145809.1(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.1(MYH14):c.3680+9C>T rs76579307
NM_001145809.1(MYH14):c.4255C>T (p.Arg1419Trp) rs115019972
NM_001145809.1(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363
NM_001145809.1(MYH14):c.4741G>A (p.Val1581Ile) rs680446
NM_001145809.1(MYH14):c.474T>C (p.Ile158=) rs34796700
NM_001145809.1(MYH14):c.4752+16G>A rs10406788
NM_001145809.1(MYH14):c.4753-9C>T rs45591233
NM_001145809.1(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_001145809.1(MYH14):c.5281C>A (p.Arg1761=) rs116035034
NM_001145809.1(MYH14):c.5430G>A (p.Ser1810=) rs3745509
NM_001145809.1(MYH14):c.5469+16C>T rs3745510
NM_001145809.1(MYH14):c.5533C>T (p.Arg1845Trp) rs199600574
NM_001145809.1(MYH14):c.5573G>A (p.Arg1858His) rs11882073
NM_001145809.1(MYH14):c.5678+12C>T rs3826772
NM_001145809.1(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_001145809.1(MYH14):c.5991G>A (p.Thr1997=) rs181567755
NM_001145809.1(MYH14):c.657G>A (p.Ala219=) rs4801822
NM_001145809.1(MYH14):c.660G>T (p.Ser220=) rs201835322
NM_001145809.1(MYH14):c.91C>A (p.Pro31Thr) rs590722
NM_024729.3(MYH14):c.*216T>G rs627491
NM_024729.3(MYH14):c.1000C>G (p.Pro334Ala) rs34498817
NM_024729.3(MYH14):c.1010C>G (p.Ser337Cys) rs35315400
NM_024729.3(MYH14):c.1126G>T (p.Gly376Cys) rs119103280
NM_024729.3(MYH14):c.1181A>G (p.Asn394Ser) rs537153044
NM_024729.3(MYH14):c.1866C>T (p.Val622=) rs77895476
NM_024729.3(MYH14):c.2309C>T (p.Ala770Val) rs201337011
NM_024729.3(MYH14):c.2477G>A (p.Arg826His) rs547836952
NM_024729.3(MYH14):c.2718C>T (p.Arg906=) rs138987081
NM_024729.3(MYH14):c.2956C>T (p.Leu986=) rs113152264
NM_024729.3(MYH14):c.3414C>T (p.Ala1138=) rs559356437
NM_024729.3(MYH14):c.3540C>T (p.Asn1180=) rs78573213
NM_024729.3(MYH14):c.3626C>A (p.Ala1209Glu) rs11669191
NM_024729.3(MYH14):c.3971G>A (p.Ser1324Asn) rs202225655
NM_024729.3(MYH14):c.4463G>A (p.Arg1488His) rs185232438
NM_024729.3(MYH14):c.4473C>T (p.Ala1491=) rs35453633
NM_024729.3(MYH14):c.4630-5A>G rs118097099
NM_024729.3(MYH14):c.483G>A (p.Met161Ile) rs34773557
NM_024729.3(MYH14):c.5211T>C (p.Gly1737=) rs115844649
NM_024729.3(MYH14):c.5343G>A (p.Leu1781=) rs10419343
NM_024729.3(MYH14):c.5406C>T (p.Ser1802=) rs12610591
NM_024729.3(MYH14):c.5889A>T (p.Leu1963=) rs73932457
NM_024729.3(MYH14):c.802A>G (p.Ile268Val) rs55645295

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