ClinVar Miner

List of variants in gene MYH14 reported as likely benign

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Gene type:
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Total variants: 109
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HGVS dbSNP
NC_000019.10:g.50255268C>T
NC_000019.10:g.50293244C>T
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.1026G>A (p.Pro342=) rs368124508
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400
NM_001145809.2(MYH14):c.1114+13C>T rs11666328
NM_001145809.2(MYH14):c.1115-4C>T rs142696359
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.1155C>T (p.Asn385=) rs558991834
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044
NM_001145809.2(MYH14):c.1210+12G>A rs367560074
NM_001145809.2(MYH14):c.1275C>T (p.Thr425=) rs149221129
NM_001145809.2(MYH14):c.1301A>G (p.Tyr434Cys) rs556541366
NM_001145809.2(MYH14):c.1330-7C>T rs1455864505
NM_001145809.2(MYH14):c.1483-10G>A rs73061136
NM_001145809.2(MYH14):c.1533G>A (p.Gln511=) rs727504664
NM_001145809.2(MYH14):c.1625T>G (p.Leu542Arg) rs727504564
NM_001145809.2(MYH14):c.1626G>A (p.Leu542=) rs727504565
NM_001145809.2(MYH14):c.1665C>T (p.Pro555=) rs202104229
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.1944C>T (p.Asp648=) rs189243324
NM_001145809.2(MYH14):c.1992G>A (p.Pro664=) rs192745436
NM_001145809.2(MYH14):c.1995G>A (p.Ser665=) rs876657514
NM_001145809.2(MYH14):c.2145C>T (p.Tyr715=) rs774452001
NM_001145809.2(MYH14):c.2205C>G (p.Arg735=) rs378811
NM_001145809.2(MYH14):c.2232+9C>T rs1335453719
NM_001145809.2(MYH14):c.2334C>A (p.Leu778=) rs190941610
NM_001145809.2(MYH14):c.2359G>A (p.Glu787Lys) rs397516628
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011
NM_001145809.2(MYH14):c.2600G>A (p.Arg867His) rs547836952
NM_001145809.2(MYH14):c.2680C>A (p.Arg894=) rs34805056
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>A (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.3468-3C>T rs78192108
NM_001145809.2(MYH14):c.3514C>A (p.Arg1172=) rs373919106
NM_001145809.2(MYH14):c.3537C>T (p.Ala1179=) rs559356437
NM_001145809.2(MYH14):c.3585G>A (p.Ala1195=) rs368190437
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.3777C>T (p.His1259=) rs371116668
NM_001145809.2(MYH14):c.3778G>A (p.Gly1260Ser) rs200272339
NM_001145809.2(MYH14):c.3871G>T (p.Val1291Leu) rs202242879
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006
NM_001145809.2(MYH14):c.3987G>A (p.Gly1329=) rs876657515
NM_001145809.2(MYH14):c.4056G>A (p.Gly1352=) rs549322167
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn) rs202225655
NM_001145809.2(MYH14):c.4098G>A (p.Lys1366=) rs876657516
NM_001145809.2(MYH14):c.4107C>T (p.Ser1369=) rs372927021
NM_001145809.2(MYH14):c.4138-13C>T rs183327883
NM_001145809.2(MYH14):c.4138-4A>G rs373533012
NM_001145809.2(MYH14):c.4152G>A (p.Glu1384=) rs727504965
NM_001145809.2(MYH14):c.4377C>T (p.Ala1459=) rs779641478
NM_001145809.2(MYH14):c.4417G>A (p.Val1473Met) rs112716976
NM_001145809.2(MYH14):c.4539+10C>T rs561531825
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.4617T>G (p.Arg1539=) rs375866139
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.4752+15C>T rs745696035
NM_001145809.2(MYH14):c.4752C>T (p.Ser1584=)
NM_001145809.2(MYH14):c.4753-5A>G rs118097099
NM_001145809.2(MYH14):c.4753-9C>T rs45591233
NM_001145809.2(MYH14):c.4800T>C (p.Asn1600=) rs772671104
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557
NM_001145809.2(MYH14):c.4845G>A (p.Ala1615=) rs1386018095
NM_001145809.2(MYH14):c.4943G>A (p.Arg1648Lys) rs727503228
NM_001145809.2(MYH14):c.5076C>A (p.Ala1692=) rs727503229
NM_001145809.2(MYH14):c.5127+10G>A rs370928889
NM_001145809.2(MYH14):c.5128-11G>A rs774151356
NM_001145809.2(MYH14):c.5128-12C>T rs372261958
NM_001145809.2(MYH14):c.5207G>A (p.Ser1736Asn) rs776401666
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.534C>T (p.Thr178=) rs727503221
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.5573G>A (p.Arg1858His) rs11882073
NM_001145809.2(MYH14):c.5778C>T (p.Leu1926=) rs201839634
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_001145809.2(MYH14):c.590+13G>A rs727504954
NM_001145809.2(MYH14):c.5960+8C>T rs373176553
NM_001145809.2(MYH14):c.5961-14T>C rs757255560
NM_001145809.2(MYH14):c.5964C>T (p.Arg1988=) rs768413723
NM_001145809.2(MYH14):c.6012A>T (p.Leu2004=) rs73932457
NM_001145809.2(MYH14):c.657G>T (p.Ala219=)
NM_001145809.2(MYH14):c.660G>A (p.Ser220=) rs201835322
NM_001145809.2(MYH14):c.693+12C>T rs370673291
NM_001145809.2(MYH14):c.693+6C>T rs1057523288
NM_001145809.2(MYH14):c.810C>T (p.Phe270=) rs374146214
NM_001145809.2(MYH14):c.826A>G (p.Ile276Val) rs55645295
NM_001145809.2(MYH14):c.858C>T (p.Gly286=) rs376429869
NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr) rs590722
NM_001145809.2(MYH14):c.975C>T (p.Ala325=) rs553878240

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