ClinVar Miner

List of variants in gene MYH14 studied for not provided

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Gene type:
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Total variants: 151
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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.1026G>A (p.Pro342=) rs368124508
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400
NM_001145809.2(MYH14):c.1115-4C>T rs142696359
NM_001145809.2(MYH14):c.1115-71G>A rs600730
NM_001145809.2(MYH14):c.1133C>T (p.Ser378Leu) rs150806988
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280
NM_001145809.2(MYH14):c.1182C>T (p.Thr394=) rs749828438
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044
NM_001145809.2(MYH14):c.1210+58C>T rs114216808
NM_001145809.2(MYH14):c.1224C>T (p.Leu408=) rs145163585
NM_001145809.2(MYH14):c.1275C>T (p.Thr425=) rs149221129
NM_001145809.2(MYH14):c.1301A>G (p.Tyr434Cys) rs556541366
NM_001145809.2(MYH14):c.1397G>A (p.Arg466His)
NM_001145809.2(MYH14):c.1419C>T (p.Arg473=) rs371946306
NM_001145809.2(MYH14):c.1436C>A (p.Ala479Asp) rs886044300
NM_001145809.2(MYH14):c.1558G>A (p.Val520Met) rs754530741
NM_001145809.2(MYH14):c.1608C>T (p.Leu536=) rs769161197
NM_001145809.2(MYH14):c.1779G>A (p.Pro593=) rs557237074
NM_001145809.2(MYH14):c.1834G>A (p.Asp612Asn) rs571071269
NM_001145809.2(MYH14):c.1890C>T (p.Val630=) rs77895476
NM_001145809.2(MYH14):c.1897T>C (p.Leu633=) rs1162570765
NM_001145809.2(MYH14):c.1918C>T (p.Arg640Trp) rs376267080
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.1944C>T (p.Asp648=) rs189243324
NM_001145809.2(MYH14):c.2161C>T (p.Arg721Cys) rs373929652
NM_001145809.2(MYH14):c.2232+86T>C rs73068986
NM_001145809.2(MYH14):c.2354+47C>T rs115140652
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=) rs780830508
NM_001145809.2(MYH14):c.2547C>T (p.Val849=) rs1159355381
NM_001145809.2(MYH14):c.2600G>A (p.Arg867His) rs547836952
NM_001145809.2(MYH14):c.2680C>A (p.Arg894=) rs34805056
NM_001145809.2(MYH14):c.2695-90G>A rs3745502
NM_001145809.2(MYH14):c.2763A>G (p.Lys921=) rs191788683
NM_001145809.2(MYH14):c.276G>A (p.Pro92=) rs913915720
NM_001145809.2(MYH14):c.2792G>A (p.Arg931His) rs200351672
NM_001145809.2(MYH14):c.2826+10C>G rs1236916887
NM_001145809.2(MYH14):c.2840G>A (p.Arg947His) rs374883445
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081
NM_001145809.2(MYH14):c.2921G>A (p.Arg974His) rs113993956
NM_001145809.2(MYH14):c.293G>A (p.Arg98His) rs370947453
NM_001145809.2(MYH14):c.3034-85G>A rs936021
NM_001145809.2(MYH14):c.3098C>T (p.Thr1033Met) rs201746408
NM_001145809.2(MYH14):c.327C>T (p.Asp109=) rs780322540
NM_001145809.2(MYH14):c.3303A>G (p.Leu1101=) rs543799021
NM_001145809.2(MYH14):c.3363G>C (p.Glu1121Asp) rs374915603
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.3401A>G (p.Gln1134Arg) rs934260773
NM_001145809.2(MYH14):c.3467+9T>G rs1378826651
NM_001145809.2(MYH14):c.3468-3C>T rs78192108
NM_001145809.2(MYH14):c.3514C>A (p.Arg1172=) rs373919106
NM_001145809.2(MYH14):c.351C>T (p.Asn117=) rs755596399
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.36G>A (p.Lys12=) rs372741317
NM_001145809.2(MYH14):c.3705G>A (p.Thr1235=) rs775178805
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191
NM_001145809.2(MYH14):c.3756G>A (p.Val1252=) rs368640289
NM_001145809.2(MYH14):c.3778G>A (p.Gly1260Ser) rs200272339
NM_001145809.2(MYH14):c.3798G>A (p.Leu1266=) rs1601005216
NM_001145809.2(MYH14):c.3819C>T (p.Ala1273=) rs750779364
NM_001145809.2(MYH14):c.3825+7T>G rs1353379371
NM_001145809.2(MYH14):c.3837A>G (p.Ala1279=)
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.4011T>G (p.Ala1337=)
NM_001145809.2(MYH14):c.4032+52G>C rs1077990
NM_001145809.2(MYH14):c.4033-7C>T rs751864175
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.408G>A (p.Thr136=) rs376120352
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn) rs202225655
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.4255C>T (p.Arg1419Trp) rs115019972
NM_001145809.2(MYH14):c.4296C>T (p.Ser1432=) rs370811348
NM_001145809.2(MYH14):c.4377C>T (p.Ala1459=) rs779641478
NM_001145809.2(MYH14):c.4413G>A (p.Glu1471=) rs771604158
NM_001145809.2(MYH14):c.4417G>A (p.Val1473Met) rs112716976
NM_001145809.2(MYH14):c.4445G>A (p.Arg1482Gln) rs746594902
NM_001145809.2(MYH14):c.4467C>T (p.Asp1489=) rs746379075
NM_001145809.2(MYH14):c.4586G>A (p.Arg1529His) rs185232438
NM_001145809.2(MYH14):c.4596C>T (p.Ala1532=) rs35453633
NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=) rs375866139
NM_001145809.2(MYH14):c.4705G>T (p.Ala1569Ser) rs145522874
NM_001145809.2(MYH14):c.4732A>G (p.Lys1578Glu) rs1601027737
NM_001145809.2(MYH14):c.4740C>T (p.Asp1580=) rs751909208
NM_001145809.2(MYH14):c.4741G>A (p.Val1581Ile) rs680446
NM_001145809.2(MYH14):c.474T>C (p.Ile158=) rs34796700
NM_001145809.2(MYH14):c.4752+16G>A rs10406788
NM_001145809.2(MYH14):c.4752C>T (p.Ser1584=) rs377081835
NM_001145809.2(MYH14):c.4753-5A>G rs118097099
NM_001145809.2(MYH14):c.4753-9C>T rs45591233
NM_001145809.2(MYH14):c.4808G>A (p.Arg1603Gln) rs886043615
NM_001145809.2(MYH14):c.4824A>G (p.Glu1608=) rs375214134
NM_001145809.2(MYH14):c.4827G>A (p.Leu1609=) rs201418071
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.4943G>A (p.Arg1648Lys) rs727503228
NM_001145809.2(MYH14):c.4950G>A (p.Arg1650=) rs763245691
NM_001145809.2(MYH14):c.5041G>A (p.Glu1681Lys) rs556548077
NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.2(MYH14):c.5121G>A (p.Lys1707=) rs1054806111
NM_001145809.2(MYH14):c.5127+10G>A rs370928889
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.5227C>T (p.Leu1743=) rs147447646
NM_001145809.2(MYH14):c.5244G>A (p.Leu1748=) rs201101562
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.5302C>T (p.Arg1768Trp) rs766866459
NM_001145809.2(MYH14):c.5334T>C (p.Gly1778=) rs115844649
NM_001145809.2(MYH14):c.5401G>A (p.Glu1801Lys) rs771246753
NM_001145809.2(MYH14):c.5452C>T (p.Arg1818Cys) rs377096949
NM_001145809.2(MYH14):c.5463C>T (p.Leu1821=) rs370616094
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.565C>T (p.Arg189Cys) rs200818171
NM_001145809.2(MYH14):c.5683C>T (p.Arg1895Cys) rs200485394
NM_001145809.2(MYH14):c.5707C>T (p.Arg1903Cys) rs372637743
NM_001145809.2(MYH14):c.5778C>T (p.Leu1926=) rs201839634
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.5960+8C>T rs373176553
NM_001145809.2(MYH14):c.5963G>A (p.Arg1988His) rs376315069
NM_001145809.2(MYH14):c.5964C>T (p.Arg1988=) rs768413723
NM_001145809.2(MYH14):c.6012A>T (p.Leu2004=) rs73932457
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=) rs4801822
NM_001145809.2(MYH14):c.660G>A (p.Ser220=) rs201835322
NM_001145809.2(MYH14):c.660G>T (p.Ser220=) rs201835322
NM_001145809.2(MYH14):c.693+10C>T rs186027440
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

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