ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280 0.00303
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646 0.00218
NM_001145809.2(MYH14):c.3079C>T (p.Leu1027=) rs113152264 0.00210
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363 0.00158
NM_001145809.2(MYH14):c.5127+10G>A rs370928889 0.00153
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073 0.00137
NM_001145809.2(MYH14):c.1944C>T (p.Asp648=) rs189243324 0.00120
NM_001145809.2(MYH14):c.4417G>A (p.Val1473Met) rs112716976 0.00107
NM_001145809.2(MYH14):c.1275C>T (p.Thr425=) rs149221129 0.00098
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011 0.00093
NM_001145809.2(MYH14):c.1992G>A (p.Pro664=) rs192745436 0.00086
NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=) rs375866139 0.00075
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006 0.00071
NM_001145809.2(MYH14):c.2680C>A (p.Arg894=) rs34805056 0.00062
NM_001145809.2(MYH14):c.5778C>T (p.Leu1926=) rs201839634 0.00039
NM_001145809.2(MYH14):c.1115-4C>T rs142696359 0.00036
NM_001145809.2(MYH14):c.5960+8C>T rs373176553 0.00034
NM_001145809.2(MYH14):c.1026G>A (p.Pro342=) rs368124508 0.00029
NM_001145809.2(MYH14):c.4943G>A (p.Arg1648Lys) rs727503228 0.00023
NM_001145809.2(MYH14):c.1155C>T (p.Asn385=) rs558991834 0.00022
NM_001145809.2(MYH14):c.1994C>T (p.Ser665Leu) rs373698416 0.00021
NM_001145809.2(MYH14):c.3514C>A (p.Arg1172=) rs373919106 0.00016
NM_001145809.2(MYH14):c.1210+12G>A rs367560074 0.00015
NM_001145809.2(MYH14):c.858C>T (p.Gly286=) rs376429869 0.00014
NM_001145809.2(MYH14):c.810C>T (p.Phe270=) rs374146214 0.00013
NM_001145809.2(MYH14):c.1301A>G (p.Tyr434Cys) rs556541366 0.00012
NM_001145809.2(MYH14):c.693+12C>T rs370673291 0.00009
NM_001145809.2(MYH14):c.3778G>A (p.Gly1260Ser) rs200272339 0.00008
NM_001145809.2(MYH14):c.3777C>T (p.His1259=) rs371116668 0.00007
NM_001145809.2(MYH14):c.4800T>C (p.Asn1600=) rs772671104 0.00007
NM_001145809.2(MYH14):c.2334C>A (p.Leu778=) rs190941610 0.00006
NM_001145809.2(MYH14):c.5128-11G>A rs774151356 0.00006
NM_001145809.2(MYH14):c.5128-12C>T rs372261958 0.00006
NM_001145809.2(MYH14):c.3537C>T (p.Ala1179=) rs559356437 0.00005
NM_001145809.2(MYH14):c.4377C>T (p.Ala1459=) rs779641478 0.00005
NM_001145809.2(MYH14):c.1665C>T (p.Pro555=) rs202104229 0.00004
NM_001145809.2(MYH14):c.3585G>A (p.Ala1195=) rs368190437 0.00004
NM_001145809.2(MYH14):c.975C>T (p.Ala325=) rs553878240 0.00004
NM_001145809.2(MYH14):c.1626G>A (p.Leu542=) rs727504565 0.00003
NM_001145809.2(MYH14):c.4056G>A (p.Gly1352=) rs549322167 0.00003
NM_001145809.2(MYH14):c.4107C>T (p.Ser1369=) rs372927021 0.00003
NM_001145809.2(MYH14):c.4539+10C>T rs561531825 0.00003
NM_001145809.2(MYH14):c.1251G>A (p.Thr417=) rs759132835 0.00002
NM_001145809.2(MYH14):c.4259C>T (p.Ala1420Val) rs727503225 0.00002
NM_001145809.2(MYH14):c.4752+15C>T rs745696035 0.00002
NM_001145809.2(MYH14):c.4845G>A (p.Ala1615=) rs1386018095 0.00002
NM_001145809.2(MYH14):c.5207G>A (p.Ser1736Asn) rs776401666 0.00002
NM_001145809.2(MYH14):c.5553G>A (p.Gln1851=) rs748686805 0.00002
NM_001145809.2(MYH14):c.1995G>A (p.Ser665=) rs876657514 0.00001
NM_001145809.2(MYH14):c.2145C>T (p.Tyr715=) rs774452001 0.00001
NM_001145809.2(MYH14):c.2733G>A (p.Val911=) rs1330663203 0.00001
NM_001145809.2(MYH14):c.4138-4A>G rs373533012 0.00001
NM_001145809.2(MYH14):c.534C>T (p.Thr178=) rs727503221 0.00001
NM_001145809.2(MYH14):c.1330-7C>T rs1455864505
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.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.2232+9C>T rs1335453719
NM_001145809.2(MYH14):c.2585+12C>T
NM_001145809.2(MYH14):c.33G>A (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.3987G>A (p.Gly1329=) rs876657515
NM_001145809.2(MYH14):c.4098G>A (p.Lys1366=) rs876657516
NM_001145809.2(MYH14):c.4152G>A (p.Glu1384=) rs727504965
NM_001145809.2(MYH14):c.5076C>A (p.Ala1692=) rs727503229
NM_001145809.2(MYH14):c.5268C>T (p.Ala1756=) rs919018072
NM_001145809.2(MYH14):c.590+13G>A rs727504954
NM_001145809.2(MYH14):c.5961-14T>C rs757255560
NM_001145809.2(MYH14):c.660G>A (p.Ser220=) rs201835322
NM_001145809.2(MYH14):c.66G>A (p.Glu22=) rs2032117052
NM_001145809.2(MYH14):c.693+6C>T rs1057523288

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