ClinVar Miner

List of variants in gene MYH14 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081 0.01050
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624 0.00710
NM_001145809.2(MYH14):c.2792G>A (p.Arg931His) rs200351672 0.00460
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280 0.00303
NM_001145809.2(MYH14):c.973+333G>A rs546221244 0.00265
NM_001145809.2(MYH14):c.1329+15C>T rs200176028 0.00227
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646 0.00218
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn) rs202225655 0.00134
NM_001145809.2(MYH14):c.1992G>A (p.Pro664=) rs192745436 0.00086
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006 0.00071
NM_001145809.2(MYH14):c.3850C>T (p.Arg1284Trp) rs201515738 0.00037
NM_001145809.2(MYH14):c.1115-4C>T rs142696359 0.00036
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val) rs200424400 0.00027
NM_001145809.2(MYH14):c.3871G>T (p.Val1291Leu) rs202242879 0.00024
NM_001145809.2(MYH14):c.1994C>T (p.Ser665Leu) rs373698416 0.00021
NM_001145809.2(MYH14):c.2645C>T (p.Ala882Val) rs202065396 0.00021
NM_001145809.2(MYH14):c.2840G>A (p.Arg947His) rs374883445 0.00018
NM_001145809.2(MYH14):c.4028C>T (p.Ala1343Val) rs374058410 0.00017
NM_001145809.2(MYH14):c.3098C>T (p.Thr1033Met) rs201746408 0.00015
NM_001145809.2(MYH14):c.2331C>T (p.Ile777=) rs746261612 0.00014
NM_001145809.2(MYH14):c.4827G>A (p.Leu1609=) rs201418071 0.00014
NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr) rs138001307 0.00014
NM_001145809.2(MYH14):c.1229G>A (p.Arg410His) rs374720181 0.00013
NM_001145809.2(MYH14):c.2864G>A (p.Arg955Gln) rs576611342 0.00013
NM_001145809.2(MYH14):c.810C>T (p.Phe270=) rs374146214 0.00013
NM_001145809.2(MYH14):c.5876G>A (p.Arg1959Gln) rs200878464 0.00012
NM_001145809.2(MYH14):c.4731C>T (p.Ser1577=) rs766728732 0.00011
NM_001145809.2(MYH14):c.693C>T (p.Pro231=) rs373744231 0.00009
NM_001145809.2(MYH14):c.3778G>A (p.Gly1260Ser) rs200272339 0.00008
NM_001145809.2(MYH14):c.4467C>T (p.Asp1489=) rs746379075 0.00007
NM_001145809.2(MYH14):c.4220G>A (p.Arg1407His) rs553162373 0.00005
NM_001145809.2(MYH14):c.1558G>A (p.Val520Met) rs754530741 0.00004
NM_001145809.2(MYH14):c.1779G>A (p.Pro593=) rs557237074 0.00004
NM_001145809.2(MYH14):c.4296C>T (p.Ser1432=) rs370811348 0.00004
NM_001145809.2(MYH14):c.5105T>C (p.Val1702Ala) rs775130663 0.00004
NM_001145809.2(MYH14):c.1397G>A (p.Arg466His) rs757828611 0.00003
NM_001145809.2(MYH14):c.1655C>T (p.Pro552Leu) rs727505282 0.00003
NM_001145809.2(MYH14):c.293G>A (p.Arg98His) rs370947453 0.00002
NM_001145809.2(MYH14):c.3599G>A (p.Arg1200Gln) rs573195811 0.00002
NM_001145809.2(MYH14):c.4585C>T (p.Arg1529Cys) rs758821769 0.00002
NM_001145809.2(MYH14):c.3194G>A (p.Arg1065His) rs769362736 0.00001
NM_001145809.2(MYH14):c.3837A>G (p.Ala1279=) rs758309547 0.00001
NM_001145809.2(MYH14):c.4011T>G (p.Ala1337=) rs1305383726 0.00001
NM_001145809.2(MYH14):c.4849G>A (p.Glu1617Lys) rs553038266 0.00001
NM_001145809.2(MYH14):c.6088T>A (p.Ser2030Thr) rs727503231 0.00001
NM_001145809.2(MYH14):c.94C>T (p.Arg32Cys) rs549293063 0.00001
NM_001145809.2(MYH14):c.1038C>A (p.Pro346=)
NM_001145809.2(MYH14):c.1074G>A (p.Glu358=)
NM_001145809.2(MYH14):c.1521C>T (p.Asn507=)
NM_001145809.2(MYH14):c.1618C>T (p.Leu540Phe)
NM_001145809.2(MYH14):c.1625T>G (p.Leu542Arg) rs727504564
NM_001145809.2(MYH14):c.1849G>A (p.Glu617Lys)
NM_001145809.2(MYH14):c.1887C>T (p.Asn629=)
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.1955del (p.Gly652fs) rs1401235358
NM_001145809.2(MYH14):c.2298C>T (p.Ile766=)
NM_001145809.2(MYH14):c.2570G>A (p.Gly857Glu)
NM_001145809.2(MYH14):c.2718G>A (p.Thr906=)
NM_001145809.2(MYH14):c.3105G>A (p.Glu1035=)
NM_001145809.2(MYH14):c.3346C>T (p.Arg1116Trp)
NM_001145809.2(MYH14):c.359C>T (p.Ser120Leu) rs119103281
NM_001145809.2(MYH14):c.390C>T (p.Tyr130=) rs2123157519
NM_001145809.2(MYH14):c.4194C>T (p.Ala1398=) rs2123419789
NM_001145809.2(MYH14):c.4213G>T (p.Gly1405Trp)
NM_001145809.2(MYH14):c.4218G>A (p.Leu1406=)
NM_001145809.2(MYH14):c.4260G>A (p.Ala1420=)
NM_001145809.2(MYH14):c.4614G>A (p.Glu1538=)
NM_001145809.2(MYH14):c.4664A>C (p.Glu1555Ala)
NM_001145809.2(MYH14):c.4732A>G (p.Lys1578Glu) rs1601027737
NM_001145809.2(MYH14):c.4966-2A>G
NM_001145809.2(MYH14):c.5030G>T (p.Arg1677Leu) rs377399732
NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.2(MYH14):c.5281C>T (p.Arg1761Trp) rs116035034
NM_001145809.2(MYH14):c.5302C>T (p.Arg1768Trp) rs766866459
NM_001145809.2(MYH14):c.5707C>T (p.Arg1903Cys) rs372637743
NM_001145809.2(MYH14):c.5923A>G (p.Met1975Val)
NM_001145809.2(MYH14):c.5991_5992insCACCACCTGGCGCGCACG (p.Thr1997_Val1998insHisHisLeuAlaArgThr)
NM_001145809.2(MYH14):c.6096A>C (p.Pro2032=) rs2036794131
NM_001145809.2(MYH14):c.677A>C (p.Lys226Thr)
NM_001145809.2(MYH14):c.973+233C>T
NM_001145809.2(MYH14):c.973+268G>A
NM_001145809.2(MYH14):c.973+374C>T

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