ClinVar Miner

List of variants in gene MYLK reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP
NM_053025.4(MYLK):c.1113G>A (p.Arg371=) rs139391789
NM_053025.4(MYLK):c.1132C>G (p.Arg378Gly) rs11920433
NM_053025.4(MYLK):c.1167G>A (p.Leu389=) rs377631029
NM_053025.4(MYLK):c.1179_1181TGT[1] (p.Val395del) rs771815695
NM_053025.4(MYLK):c.1212C>A (p.Pro404=) rs765597431
NM_053025.4(MYLK):c.1212C>T (p.Pro404=) rs765597431
NM_053025.4(MYLK):c.1356C>T (p.Thr452=) rs768697251
NM_053025.4(MYLK):c.1359C>T (p.Pro453=) rs200973568
NM_053025.4(MYLK):c.1420C>T (p.Leu474=) rs1413024663
NM_053025.4(MYLK):c.1473C>T (p.Asn491=) rs138761352
NM_053025.4(MYLK):c.1752A>G (p.Leu584=) rs775877814
NM_053025.4(MYLK):c.1785C>T (p.Ser595=) rs370094325
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.2061G>A (p.Pro687=) rs539307414
NM_053025.4(MYLK):c.2076G>A (p.Thr692=) rs147295583
NM_053025.4(MYLK):c.2125G>A (p.Val709Met) rs112537316
NM_053025.4(MYLK):c.2127G>A (p.Val709=) rs138575251
NM_053025.4(MYLK):c.2140+6G>A rs374346618
NM_053025.4(MYLK):c.2253C>T (p.Thr751=) rs138777049
NM_053025.4(MYLK):c.225C>T (p.Ser75=) rs371699704
NM_053025.4(MYLK):c.2485G>A (p.Glu829Lys) rs370190691
NM_053025.4(MYLK):c.256C>T (p.Arg86Trp) rs368822172
NM_053025.4(MYLK):c.2595C>T (p.Asp865=) rs567610011
NM_053025.4(MYLK):c.2604C>T (p.Asp868=) rs372924929
NM_053025.4(MYLK):c.2652G>A (p.Glu884=) rs1314650520
NM_053025.4(MYLK):c.2799G>A (p.Val933=) rs144806671
NM_053025.4(MYLK):c.2898C>T (p.Pro966=) rs753785049
NM_053025.4(MYLK):c.2918C>T (p.Pro973Leu) rs760450984
NM_053025.4(MYLK):c.2919G>A (p.Pro973=) rs149482336
NM_053025.4(MYLK):c.3000C>T (p.Ala1000=) rs141546581
NM_053025.4(MYLK):c.3120C>T (p.Asn1040=) rs759475810
NM_053025.4(MYLK):c.3336C>A (p.Gly1112=) rs1060504648
NM_053025.4(MYLK):c.3351C>A (p.Leu1117=) rs1240784181
NM_053025.4(MYLK):c.3397C>T (p.Leu1133=) rs1060504649
NM_053025.4(MYLK):c.3438C>T (p.Leu1146=) rs146320279
NM_053025.4(MYLK):c.3449-11_3449-9del rs952172362
NM_053025.4(MYLK):c.3462C>T (p.Ser1154=) rs768346816
NM_053025.4(MYLK):c.3495A>G (p.Arg1165=) rs142345443
NM_053025.4(MYLK):c.3639G>A (p.Val1213=) rs148419939
NM_053025.4(MYLK):c.3653-10_3653-8del rs576620371
NM_053025.4(MYLK):c.3660G>A (p.Ala1220=) rs765219262
NM_053025.4(MYLK):c.3681C>T (p.Ala1227=) rs201663473
NM_053025.4(MYLK):c.3706A>G (p.Met1236Val) rs113124819
NM_053025.4(MYLK):c.3750C>T (p.Arg1250=) rs201873975
NM_053025.4(MYLK):c.3832-6C>T rs185681684
NM_053025.4(MYLK):c.3898G>A (p.Ala1300Thr) rs149530842
NM_053025.4(MYLK):c.3915C>T (p.Cys1305=) rs371602931
NM_053025.4(MYLK):c.4119A>G (p.Ser1373=) rs758896854
NM_053025.4(MYLK):c.4131G>A (p.Thr1377=) rs756697460
NM_053025.4(MYLK):c.4170C>T (p.Asn1390=) rs545959628
NM_053025.4(MYLK):c.4195G>A (p.Glu1399Lys) rs181663420
NM_053025.4(MYLK):c.4221C>A (p.Ile1407=) rs780641277
NM_053025.4(MYLK):c.423-8C>T rs751696363
NM_053025.4(MYLK):c.4293G>A (p.Pro1431=) rs370153686
NM_053025.4(MYLK):c.4302A>G (p.Glu1434=) rs145872838
NM_053025.4(MYLK):c.4335C>T (p.Pro1445=) rs756038706
NM_053025.4(MYLK):c.4392C>T (p.Tyr1464=) rs565217509
NM_053025.4(MYLK):c.465C>A (p.Ile155=) rs199517273
NM_053025.4(MYLK):c.4725C>T (p.Tyr1575=) rs374665486
NM_053025.4(MYLK):c.4838-7G>A rs377561378
NM_053025.4(MYLK):c.4908G>A (p.Glu1636=) rs1553777406
NM_053025.4(MYLK):c.4920C>T (p.Tyr1640=) rs756699701
NM_053025.4(MYLK):c.4929C>T (p.Asp1643=) rs138423692
NM_053025.4(MYLK):c.4941C>T (p.Ile1647=) rs200291268
NM_053025.4(MYLK):c.5001C>T (p.Asn1667=) rs375038682
NM_053025.4(MYLK):c.5019T>C (p.Val1673=) rs1553774768
NM_053025.4(MYLK):c.5114+7A>G rs1553774672
NM_053025.4(MYLK):c.5114+8G>A rs202229368
NM_053025.4(MYLK):c.5121C>T (p.Arg1707=) rs144436556
NM_053025.4(MYLK):c.5166T>C (p.Asp1722=) rs140870383
NM_053025.4(MYLK):c.5369-10T>G rs373584324
NM_053025.4(MYLK):c.5535T>C (p.Asp1845=) rs748934365
NM_053025.4(MYLK):c.5562C>T (p.His1854=) rs199880151
NM_053025.4(MYLK):c.5715T>G (p.Gly1905=) rs753024354
NM_053025.4(MYLK):c.711C>T (p.Asn237=) rs149407805
NM_053025.4(MYLK):c.716C>T (p.Ser239Leu) rs137982786
NM_053025.4(MYLK):c.717G>A (p.Ser239=) rs146960026
NM_053025.4(MYLK):c.755-4C>G rs1249330032
NM_053025.4(MYLK):c.771T>C (p.Asn257=) rs369494886
NM_053025.4(MYLK):c.957G>A (p.Glu319=) rs864622770
NM_053025.4(MYLK):c.963G>A (p.Lys321=) rs1052922812
NM_053025.4(MYLK):c.96C>T (p.Ala32=) rs775979851
NM_053025.4(MYLK):c.999G>A (p.Pro333=) rs13319347

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