ClinVar Miner

List of variants in gene MYLK reported by PreventionGenetics

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Gene type:
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Total variants: 54
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HGVS dbSNP
NM_053025.3(MYLK):c.588+13_588+16delTCTG rs570821069
NM_053025.4(MYLK):c.1005C>T (p.Thr335=) rs4678047
NM_053025.4(MYLK):c.1327C>T (p.Pro443Ser) rs35156360
NM_053025.4(MYLK):c.1486C>G (p.Leu496Val) rs9833275
NM_053025.4(MYLK):c.1651+6T>A rs820329
NM_053025.4(MYLK):c.1668C>T (p.Tyr556=) rs752021743
NM_053025.4(MYLK):c.1804+8C>T rs820355
NM_053025.4(MYLK):c.207C>T (p.Asn69=) rs376457425
NM_053025.4(MYLK):c.2101G>A (p.Ala701Thr) rs142835596
NM_053025.4(MYLK):c.2127G>A (p.Val709=) rs138575251
NM_053025.4(MYLK):c.2533C>T (p.Arg845Cys) rs3732485
NM_053025.4(MYLK):c.2582T>C (p.Leu861Pro) rs3732486
NM_053025.4(MYLK):c.2628C>T (p.Arg876=) rs571744275
NM_053025.4(MYLK):c.2742C>A (p.Asp914Glu) rs3732487
NM_053025.4(MYLK):c.2919G>A (p.Pro973=) rs149482336
NM_053025.4(MYLK):c.3027G>A (p.Glu1009=) rs12172926
NM_053025.4(MYLK):c.3075C>T (p.Pro1025=) rs144885184
NM_053025.4(MYLK):c.3193_3195GAA[1] (p.Glu1066del) rs75967604
NM_053025.4(MYLK):c.3253A>G (p.Thr1085Ala) rs75370906
NM_053025.4(MYLK):c.3402C>T (p.Asn1134=) rs865358
NM_053025.4(MYLK):c.3525C>T (p.Asp1175=) rs147735490
NM_053025.4(MYLK):c.3558C>T (p.Thr1186=) rs40305
NM_053025.4(MYLK):c.3652+11G>A rs41271437
NM_053025.4(MYLK):c.3706A>G (p.Met1236Val) rs113124819
NM_053025.4(MYLK):c.373+18C>T rs140559450
NM_053025.4(MYLK):c.3832-6C>T rs185681684
NM_053025.4(MYLK):c.383C>T (p.Ala128Val) rs143896146
NM_053025.4(MYLK):c.3987T>G (p.Asp1329Glu) rs9844788
NM_053025.4(MYLK):c.411C>G (p.Ser137=) rs55760507
NM_053025.4(MYLK):c.4194C>T (p.His1398=) rs17298941
NM_053025.4(MYLK):c.4195G>A (p.Glu1399Lys) rs181663420
NM_053025.4(MYLK):c.422+14G>C rs146112057
NM_053025.4(MYLK):c.4289-10dup rs41431347
NM_053025.4(MYLK):c.4317T>C (p.Asp1439=) rs1254392
NM_053025.4(MYLK):c.439C>T (p.Pro147Ser) rs9840993
NM_053025.4(MYLK):c.4620-12G>A rs41301337
NM_053025.4(MYLK):c.4620-18G>A rs41305835
NM_053025.4(MYLK):c.4620-6C>T rs113607507
NM_053025.4(MYLK):c.4710G>A (p.Ser1570=) rs778762375
NM_053025.4(MYLK):c.4764G>A (p.Pro1588=) rs56056823
NM_053025.4(MYLK):c.479C>G (p.Pro160Arg) rs111256888
NM_053025.4(MYLK):c.4800G>A (p.Arg1600=) rs111901174
NM_053025.4(MYLK):c.4838-3C>T rs776825316
NM_053025.4(MYLK):c.4842T>C (p.Asn1614=) rs820463
NM_053025.4(MYLK):c.5001C>T (p.Asn1667=) rs375038682
NM_053025.4(MYLK):c.5114+8G>A rs202229368
NM_053025.4(MYLK):c.588+10C>T rs886038709
NM_053025.4(MYLK):c.62C>A (p.Pro21His) rs28497577
NM_053025.4(MYLK):c.639C>T (p.Asn213=) rs146073242
NM_053025.4(MYLK):c.652C>T (p.Leu218=) rs113035707
NM_053025.4(MYLK):c.754+17G>A rs146661440
NM_053025.4(MYLK):c.771T>C (p.Asn257=) rs369494886
NM_053025.4(MYLK):c.782T>C (p.Val261Ala) rs3796164
NM_053025.4(MYLK):c.999G>A (p.Pro333=) rs13319347

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