ClinVar Miner

List of variants in gene MYLK reported as uncertain significance for Cardiovascular phenotype

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Total variants: 75
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HGVS dbSNP
NM_053025.4(MYLK):c.1028G>T (p.Ser343Ile) rs961194527
NM_053025.4(MYLK):c.1075C>A (p.Pro359Thr) rs202225055
NM_053025.4(MYLK):c.1120C>T (p.Pro374Ser) rs1553822427
NM_053025.4(MYLK):c.1133G>A (p.Arg378His) rs56378658
NM_053025.4(MYLK):c.1219G>T (p.Gly407Cys) rs199719143
NM_053025.4(MYLK):c.1330G>A (p.Glu444Lys) rs766381045
NM_053025.4(MYLK):c.1375G>A (p.Gly459Ser) rs147311651
NM_053025.4(MYLK):c.1496G>C (p.Ser499Thr) rs886039189
NM_053025.4(MYLK):c.161G>A (p.Gly54Glu) rs767453947
NM_053025.4(MYLK):c.164G>A (p.Arg55Gln) rs768984022
NM_053025.4(MYLK):c.1669G>A (p.Ala557Thr) rs143403855
NM_053025.4(MYLK):c.1745C>A (p.Thr582Asn) rs749069560
NM_053025.4(MYLK):c.1786G>A (p.Ala596Thr) rs758715543
NM_053025.4(MYLK):c.1802A>C (p.His601Pro) rs45477891
NM_053025.4(MYLK):c.1957G>A (p.Glu653Lys) rs142765858
NM_053025.4(MYLK):c.1968G>T (p.Trp656Cys) rs138172035
NM_053025.4(MYLK):c.1991A>G (p.Gln664Arg) rs200273207
NM_053025.4(MYLK):c.2113C>T (p.Arg705Cys) rs547322504
NM_053025.4(MYLK):c.2125G>A (p.Val709Met) rs112537316
NM_053025.4(MYLK):c.2132C>T (p.Thr711Met) rs531232445
NM_053025.4(MYLK):c.2149G>A (p.Asp717Asn) rs150936840
NM_053025.4(MYLK):c.2182C>T (p.Arg728Cys) rs143468713
NM_053025.4(MYLK):c.226G>A (p.Gly76Arg) rs368413008
NM_053025.4(MYLK):c.2291A>G (p.Asp764Gly) rs763243524
NM_053025.4(MYLK):c.2396G>A (p.Arg799Gln) rs1435664878
NM_053025.4(MYLK):c.2474C>T (p.Pro825Leu) rs201332554
NM_053025.4(MYLK):c.256C>T (p.Arg86Trp) rs368822172
NM_053025.4(MYLK):c.257G>A (p.Arg86Gln) rs138265409
NM_053025.4(MYLK):c.2596G>A (p.Gly866Ser) rs587782966
NM_053025.4(MYLK):c.2629G>A (p.Val877Met) rs34542174
NM_053025.4(MYLK):c.2860C>T (p.Arg954Cys) rs749847711
NM_053025.4(MYLK):c.290A>C (p.His97Pro) rs756800370
NM_053025.4(MYLK):c.2936C>T (p.Pro979Leu) rs368229473
NM_053025.4(MYLK):c.3020C>T (p.Ala1007Val) rs1382043515
NM_053025.4(MYLK):c.3052C>T (p.Gln1018Ter) rs377568543
NM_053025.4(MYLK):c.3062G>C (p.Gly1021Ala) rs200041144
NM_053025.4(MYLK):c.3076G>A (p.Val1026Met) rs778578954
NM_053025.4(MYLK):c.3096_3131del (p.1032_1043AETLKPMGNAKP[1]) rs758966808
NM_053025.4(MYLK):c.3273_3274AG[2] (p.Ser1093fs) rs1553803217
NM_053025.4(MYLK):c.3472G>A (p.Glu1158Lys) rs867887039
NM_053025.4(MYLK):c.3479C>T (p.Ala1160Val) rs1222534732
NM_053025.4(MYLK):c.3526G>A (p.Ala1176Thr) rs758839208
NM_053025.4(MYLK):c.3611G>A (p.Arg1204Gln) rs142421063
NM_053025.4(MYLK):c.3637G>A (p.Val1213Met) rs368390254
NM_053025.4(MYLK):c.3659C>T (p.Ala1220Val) rs370872760
NM_053025.4(MYLK):c.3749G>A (p.Arg1250His) rs139817477
NM_053025.4(MYLK):c.3755G>A (p.Gly1252Glu) rs886039046
NM_053025.4(MYLK):c.3805T>C (p.Cys1269Arg) rs750286831
NM_053025.4(MYLK):c.3831+5G>A rs1198605932
NM_053025.4(MYLK):c.3844G>A (p.Glu1282Lys) rs765252740
NM_053025.4(MYLK):c.3898G>A (p.Ala1300Thr) rs149530842
NM_053025.4(MYLK):c.3982G>A (p.Val1328Met) rs730880164
NM_053025.4(MYLK):c.4031G>A (p.Arg1344Gln) rs774223564
NM_053025.4(MYLK):c.4082G>A (p.Ser1361Asn) rs886039143
NM_053025.4(MYLK):c.4336G>A (p.Glu1446Lys) rs146682969
NM_053025.4(MYLK):c.4348C>T (p.Arg1450Trp) rs143258617
NM_053025.4(MYLK):c.4367C>A (p.Thr1456Asn) rs1553781315
NM_053025.4(MYLK):c.4369G>A (p.Glu1457Lys) rs1018778128
NM_053025.4(MYLK):c.4520G>A (p.Arg1507Gln) rs574296889
NM_053025.4(MYLK):c.455G>A (p.Arg152His) rs201754358
NM_053025.4(MYLK):c.4565T>C (p.Val1522Ala) rs763880352
NM_053025.4(MYLK):c.4620-4G>A rs371533014
NM_053025.4(MYLK):c.4645C>T (p.Arg1549Cys) rs886039186
NM_053025.4(MYLK):c.4744G>A (p.Val1582Met) rs755510742
NM_053025.4(MYLK):c.4915G>C (p.Gly1639Arg) rs143900788
NM_053025.4(MYLK):c.5237A>C (p.Gln1746Pro) rs1226517649
NM_053025.4(MYLK):c.5264T>C (p.Ile1755Thr) rs759291796
NM_053025.4(MYLK):c.5426C>G (p.Pro1809Arg) rs1553770523
NM_053025.4(MYLK):c.5477C>T (p.Ala1826Val) rs147187907
NM_053025.4(MYLK):c.5501-3C>T rs747326867
NM_053025.4(MYLK):c.5695G>A (p.Val1899Met) rs1553768575
NM_053025.4(MYLK):c.569C>T (p.Pro190Leu) rs199736263
NM_053025.4(MYLK):c.5706G>A (p.Met1902Ile) rs1194619668
NM_053025.4(MYLK):c.619G>A (p.Val207Met) rs756560698
NM_053025.4(MYLK):c.844G>A (p.Glu282Lys) rs746464484

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