ClinVar Miner

List of variants in gene MYH14 reported as likely benign for not specified

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Total variants: 67
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HGVS dbSNP
NM_001145809.1(MYH14):c.1115-4C>T rs142696359
NM_001145809.1(MYH14):c.1155C>T (p.Asn385=) rs558991834
NM_001145809.1(MYH14):c.1210+12G>A rs367560074
NM_001145809.1(MYH14):c.1275C>T (p.Thr425=) rs149221129
NM_001145809.1(MYH14):c.1301A>G (p.Tyr434Cys) rs556541366
NM_001145809.1(MYH14):c.1330-7C>T rs1455864505
NM_001145809.1(MYH14):c.1533G>A (p.Gln511=) rs727504664
NM_001145809.1(MYH14):c.1625T>G (p.Leu542Arg) rs727504564
NM_001145809.1(MYH14):c.1626G>A (p.Leu542=) rs727504565
NM_001145809.1(MYH14):c.1665C>T (p.Pro555=) rs202104229
NM_001145809.1(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.1(MYH14):c.1944C>T (p.Asp648=) rs189243324
NM_001145809.1(MYH14):c.1992G>A (p.Pro664=) rs192745436
NM_001145809.1(MYH14):c.1995G>A (p.Ser665=) rs876657514
NM_001145809.1(MYH14):c.2145C>T (p.Tyr715=) rs774452001
NM_001145809.1(MYH14):c.2232+9C>T rs1335453719
NM_001145809.1(MYH14):c.2680C>A (p.Arg894=) rs34805056
NM_001145809.1(MYH14):c.33G>A (p.Arg11=) rs8106196
NM_001145809.1(MYH14):c.3514C>A (p.Arg1172=) rs373919106
NM_001145809.1(MYH14):c.3585G>A (p.Ala1195=) rs368190437
NM_001145809.1(MYH14):c.3777C>T (p.His1259=) rs371116668
NM_001145809.1(MYH14):c.394G>A (p.Gly132Ser) rs199910006
NM_001145809.1(MYH14):c.3987G>A (p.Gly1329=) rs876657515
NM_001145809.1(MYH14):c.4056G>A (p.Gly1352=) rs549322167
NM_001145809.1(MYH14):c.4098G>A (p.Lys1366=) rs876657516
NM_001145809.1(MYH14):c.4107C>T (p.Ser1369=) rs372927021
NM_001145809.1(MYH14):c.4138-4A>G rs373533012
NM_001145809.1(MYH14):c.4152G>A (p.Glu1384=) rs727504965
NM_001145809.1(MYH14):c.4377C>T (p.Ala1459=) rs779641478
NM_001145809.1(MYH14):c.4417G>A (p.Val1473Met) rs112716976
NM_001145809.1(MYH14):c.4617T>G (p.Arg1539=) rs375866139
NM_001145809.1(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363
NM_001145809.1(MYH14):c.4752+15C>T rs745696035
NM_001145809.1(MYH14):c.4800T>C (p.Asn1600=) rs772671104
NM_001145809.1(MYH14):c.4943G>A (p.Arg1648Lys) rs727503228
NM_001145809.1(MYH14):c.5076C>A (p.Ala1692=) rs727503229
NM_001145809.1(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.1(MYH14):c.5127+10G>A rs370928889
NM_001145809.1(MYH14):c.5128-11G>A rs774151356
NM_001145809.1(MYH14):c.5128-12C>T rs372261958
NM_001145809.1(MYH14):c.5207G>A (p.Ser1736Asn) rs776401666
NM_001145809.1(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_001145809.1(MYH14):c.534C>T (p.Thr178=) rs727503221
NM_001145809.1(MYH14):c.5573G>A (p.Arg1858His) rs11882073
NM_001145809.1(MYH14):c.5778C>T (p.Leu1926=) rs201839634
NM_001145809.1(MYH14):c.590+13G>A rs727504954
NM_001145809.1(MYH14):c.5960+8C>T rs373176553
NM_001145809.1(MYH14):c.5961-14T>C rs757255560
NM_001145809.1(MYH14):c.660G>A (p.Ser220=) rs201835322
NM_001145809.1(MYH14):c.693+12C>T rs370673291
NM_001145809.1(MYH14):c.858C>T (p.Gly286=) rs376429869
NM_001145809.1(MYH14):c.975C>T (p.Ala325=) rs553878240
NM_024729.3(MYH14):c.1002G>A (p.Pro334=) rs368124508
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.2211C>A (p.Leu737=) rs190941610
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.3655G>A (p.Gly1219Ser) rs200272339
NM_024729.3(MYH14):c.3748G>T (p.Val1250Leu) rs202242879
NM_024729.3(MYH14):c.4416+10C>T rs561531825
NM_024729.3(MYH14):c.4463G>A (p.Arg1488His) rs185232438
NM_024729.3(MYH14):c.4722G>A (p.Ala1574=) rs1386018095
NM_024729.3(MYH14):c.5841C>T (p.Arg1947=) rs768413723
NM_024729.3(MYH14):c.693+6C>T rs1057523288
NM_024729.3(MYH14):c.786C>T (p.Phe262=) rs374146214
NM_024729.3(MYH14):c.802A>G (p.Ile268Val) rs55645295

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