ClinVar Miner

List of variants in gene MYH14 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.2041G>C (p.Gly681Arg) rs75915336 0.02765
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191 0.01884
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817 0.01645
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557 0.01615
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081 0.01050
NM_001145809.2(MYH14):c.5466G>A (p.Leu1822=) rs10419343 0.01020
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.826A>G (p.Ile276Val) rs55645295 0.00445
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280 0.00303
NM_001145809.2(MYH14):c.5529C>T (p.Ser1843=) rs12610591 0.00248
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363 0.00158
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073 0.00137
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006 0.00071
NM_001145809.2(MYH14):c.2233-13C>A rs368249273 0.00034
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.3098C>T (p.Thr1033Met) rs201746408 0.00015
NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr) rs138001307 0.00014
NM_001145809.2(MYH14):c.1067C>T (p.Thr356Met) rs151082668 0.00011
NM_001145809.2(MYH14):c.266T>C (p.Leu89Pro) rs988356194 0.00011
NM_001145809.2(MYH14):c.2651A>G (p.Tyr884Cys) rs373457292 0.00009
NM_001145809.2(MYH14):c.4156A>T (p.Thr1386Ser) rs377462520 0.00009
NM_001145809.2(MYH14):c.3433C>T (p.Arg1145Trp) rs773117828 0.00006
NM_001145809.2(MYH14):c.4219C>T (p.Arg1407Cys) rs535145284 0.00006
NM_001145809.2(MYH14):c.2458C>T (p.Arg820Cys) rs767984672 0.00005
NM_001145809.2(MYH14):c.3537C>T (p.Ala1179=) rs559356437 0.00005
NM_001145809.2(MYH14):c.1381C>T (p.Arg461Cys) rs752732851 0.00003
NM_001145809.2(MYH14):c.1418G>A (p.Arg473His) rs199812021 0.00003
NM_001145809.2(MYH14):c.5963G>A (p.Arg1988His) rs376315069 0.00003
NM_001145809.2(MYH14):c.4615C>T (p.Arg1539Cys) rs770767114 0.00002
NM_001145809.2(MYH14):c.4307G>A (p.Arg1436Gln) rs773527189 0.00001
NM_001145809.2(MYH14):c.4921C>T (p.Arg1641Cys) rs748898201 0.00001
NM_001145809.2(MYH14):c.5875C>T (p.Arg1959Trp) rs758424787 0.00001
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.2988C>G (p.Ser996Arg) rs368160641
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.5975C>T (p.Thr1992Ile) rs1555779737
NM_001145809.2(MYH14):c.6074C>T (p.Pro2025Leu) rs772690371
NM_001145809.2(MYH14):c.6096A>C (p.Pro2032=) rs2036794131

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