ClinVar Miner

List of variants in gene MYH14 studied for not provided

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Total variants: 69
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HGVS dbSNP
NM_001145809.2(MYH14):c.1006C>T (p.Arg336Trp) rs371272700
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817
NM_001145809.2(MYH14):c.1115-4C>T rs142696359
NM_001145809.2(MYH14):c.1115-71G>A
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044
NM_001145809.2(MYH14):c.1210+58C>T
NM_001145809.2(MYH14):c.1436C>A (p.Ala479Asp) rs886044300
NM_001145809.2(MYH14):c.1890C>T (p.Val630=) rs77895476
NM_001145809.2(MYH14):c.2161C>T (p.Arg721Cys) rs373929652
NM_001145809.2(MYH14):c.2232+86T>C
NM_001145809.2(MYH14):c.2354+47C>T
NM_001145809.2(MYH14):c.2359G>A (p.Glu787Lys) rs397516628
NM_001145809.2(MYH14):c.2459G>A (p.Arg820His) rs370765705
NM_001145809.2(MYH14):c.24G>T (p.Val8=)
NM_001145809.2(MYH14):c.2695-90G>A
NM_001145809.2(MYH14):c.2763A>G (p.Lys921=) rs191788683
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081
NM_001145809.2(MYH14):c.3034-85G>A
NM_001145809.2(MYH14):c.3098C>T (p.Thr1033Met) rs201746408
NM_001145809.2(MYH14):c.3363G>C (p.Glu1121Asp) rs374915603
NM_001145809.2(MYH14):c.3401A>G (p.Gln1134Arg)
NM_001145809.2(MYH14):c.3537C>T (p.Ala1179=) rs559356437
NM_001145809.2(MYH14):c.359C>T (p.Ser120Leu) rs119103281
NM_001145809.2(MYH14):c.3642G>A (p.Glu1214=) rs886044561
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191
NM_001145809.2(MYH14):c.3863A>T (p.Glu1288Val) rs1555773701
NM_001145809.2(MYH14):c.3871G>T (p.Val1291Leu) rs202242879
NM_001145809.2(MYH14):c.3884G>A (p.Arg1295Gln) rs377014092
NM_001145809.2(MYH14):c.3940C>T (p.Arg1314Cys) rs776550700
NM_001145809.2(MYH14):c.4032+52G>C
NM_001145809.2(MYH14):c.4033G>A (p.Ala1345Thr) rs148054042
NM_001145809.2(MYH14):c.407C>T (p.Thr136Met) rs1057520092
NM_001145809.2(MYH14):c.4219C>T (p.Arg1407Cys) rs535145284
NM_001145809.2(MYH14):c.4220G>A (p.Arg1407His) rs553162373
NM_001145809.2(MYH14):c.4445G>A (p.Arg1482Gln) rs746594902
NM_001145809.2(MYH14):c.4740C>T (p.Asp1580=) rs751909208
NM_001145809.2(MYH14):c.4752C>T (p.Ser1584=)
NM_001145809.2(MYH14):c.4808G>A (p.Arg1603Gln) rs886043615
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557
NM_001145809.2(MYH14):c.4849G>A (p.Glu1617Lys) rs553038266
NM_001145809.2(MYH14):c.487C>T (p.Arg163Trp) rs373470153
NM_001145809.2(MYH14):c.5176C>T (p.Arg1726Trp) rs372062358
NM_001145809.2(MYH14):c.5215C>A (p.Arg1739Ser) rs761663501
NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr) rs138001307
NM_001145809.2(MYH14):c.5281C>A (p.Arg1761=) rs116035034
NM_001145809.2(MYH14):c.5401G>A (p.Glu1801Lys)
NM_001145809.2(MYH14):c.5452C>T (p.Arg1818Cys) rs377096949
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.5707C>T (p.Arg1903Cys) rs372637743
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_001145809.2(MYH14):c.5876G>A (p.Arg1959Gln) rs200878464
NM_001145809.2(MYH14):c.590+1G>A rs371338704
NM_001145809.2(MYH14):c.5953C>T (p.Arg1985Trp) rs369147236
NM_001145809.2(MYH14):c.5963G>A (p.Arg1988His) rs376315069
NM_001145809.2(MYH14):c.6035_6037AGG[1] (p.Glu2013del) rs867351302
NM_001145809.2(MYH14):c.6074C>T (p.Pro2025Leu) rs772690371
NM_001145809.2(MYH14):c.6088T>A (p.Ser2030Thr) rs727503231
NM_001145809.2(MYH14):c.615G>A (p.Thr205=) rs199921330
NM_001145809.2(MYH14):c.657G>T (p.Ala219=)
NM_001145809.2(MYH14):c.731G>A (p.Arg244Gln) rs767108206
NM_001145809.2(MYH14):c.752C>A (p.Pro251His) rs779215539
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val) rs200424400
NM_001145809.2(MYH14):c.826A>G (p.Ile276Val) rs55645295
NM_001145809.2(MYH14):c.838G>A (p.Val280Ile) rs202246093
NM_001145809.2(MYH14):c.94C>T (p.Arg32Cys) rs549293063
NM_024729.3:c.4629+16G>A

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