ClinVar Miner

List of variants in gene MYLK reported as likely benign for Cardiovascular phenotype

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Total variants: 57
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HGVS dbSNP
NM_053025.4(MYLK):c.1007C>T (p.Pro336Leu) rs35912339
NM_053025.4(MYLK):c.1110G>A (p.Glu370=) rs886038986
NM_053025.4(MYLK):c.1132C>G (p.Arg378Gly) rs11920433
NM_053025.4(MYLK):c.1134T>C (p.Arg378=) rs886039123
NM_053025.4(MYLK):c.1221C>A (p.Gly407=) rs765175526
NM_053025.4(MYLK):c.1314C>T (p.Ser438=) rs200423954
NM_053025.4(MYLK):c.1359C>T (p.Pro453=) rs200973568
NM_053025.4(MYLK):c.1570G>A (p.Ala524Thr) rs375501508
NM_053025.4(MYLK):c.1609G>A (p.Val537Ile) rs199988497
NM_053025.4(MYLK):c.1725G>A (p.Pro575=) rs376997840
NM_053025.4(MYLK):c.1752A>G (p.Leu584=) rs775877814
NM_053025.4(MYLK):c.1821G>A (p.Arg607=) rs764273764
NM_053025.4(MYLK):c.2076G>A (p.Thr692=) rs147295583
NM_053025.4(MYLK):c.207C>T (p.Asn69=) rs376457425
NM_053025.4(MYLK):c.2149G>T (p.Asp717Tyr) rs150936840
NM_053025.4(MYLK):c.2253C>T (p.Thr751=) rs138777049
NM_053025.4(MYLK):c.2433A>G (p.Leu811=) rs1320156713
NM_053025.4(MYLK):c.24C>G (p.Ala8=) rs78118111
NM_053025.4(MYLK):c.2589G>A (p.Glu863=) rs536506601
NM_053025.4(MYLK):c.2628C>T (p.Arg876=) rs571744275
NM_053025.4(MYLK):c.2631G>A (p.Val877=) rs371542306
NM_053025.4(MYLK):c.2799G>A (p.Val933=) rs144806671
NM_053025.4(MYLK):c.2937G>A (p.Pro979=) rs146177534
NM_053025.4(MYLK):c.3000C>T (p.Ala1000=) rs141546581
NM_053025.4(MYLK):c.3048T>C (p.Asn1016=) rs758822048
NM_053025.4(MYLK):c.3126G>A (p.Lys1042=) rs1199202202
NM_053025.4(MYLK):c.3183C>T (p.Ser1061=) rs370194660
NM_053025.4(MYLK):c.3210C>T (p.Asp1070=) rs200758888
NM_053025.4(MYLK):c.3242A>G (p.His1081Arg) rs113491038
NM_053025.4(MYLK):c.333C>T (p.Gly111=) rs886039008
NM_053025.4(MYLK):c.3438C>T (p.Leu1146=) rs146320279
NM_053025.4(MYLK):c.345C>T (p.Arg115=) rs1213297212
NM_053025.4(MYLK):c.3639G>A (p.Val1213=) rs148419939
NM_053025.4(MYLK):c.3681C>T (p.Ala1227=) rs201663473
NM_053025.4(MYLK):c.3750C>T (p.Arg1250=) rs201873975
NM_053025.4(MYLK):c.3843C>T (p.Ser1281=) rs377231739
NM_053025.4(MYLK):c.3969C>T (p.Val1323=) rs192100022
NM_053025.4(MYLK):c.399G>T (p.Gln133His) rs140148380
NM_053025.4(MYLK):c.4014T>C (p.Pro1338=) rs55669734
NM_053025.4(MYLK):c.4026C>T (p.Asp1342=) rs886039112
NM_053025.4(MYLK):c.4119A>G (p.Ser1373=) rs758896854
NM_053025.4(MYLK):c.4195G>A (p.Glu1399Lys) rs181663420
NM_053025.4(MYLK):c.4289-4C>G rs376670657
NM_053025.4(MYLK):c.4293G>A (p.Pro1431=) rs370153686
NM_053025.4(MYLK):c.4341T>G (p.Val1447=) rs367629715
NM_053025.4(MYLK):c.435A>C (p.Ser145=) rs747805468
NM_053025.4(MYLK):c.4602C>T (p.Ile1534=) rs578009736
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.4764G>A (p.Pro1588=) rs56056823
NM_053025.4(MYLK):c.5121C>T (p.Arg1707=) rs144436556
NM_053025.4(MYLK):c.5586C>T (p.Asp1862=) rs563208285
NM_053025.4(MYLK):c.5631T>C (p.Asp1877=) rs772417046
NM_053025.4(MYLK):c.5673C>T (p.Ala1891=) rs769361741
NM_053025.4(MYLK):c.639C>T (p.Asn213=) rs146073242
NM_053025.4(MYLK):c.993G>A (p.Thr331=) rs55932343
NM_053025.4(MYLK):c.999G>A (p.Pro333=) rs13319347

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