ClinVar Miner

List of variants in gene MYLK reported as benign

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Gene type:
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Total variants: 66
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HGVS dbSNP
NM_053025.4(MYLK):c.*1809A>G rs6438804
NM_053025.4(MYLK):c.-197T>C rs528654061
NM_053025.4(MYLK):c.1005C>T (p.Thr335=) rs4678047
NM_053025.4(MYLK):c.1007C>T (p.Pro336Leu) rs35912339
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.1516+16C>T rs77590783
NM_053025.4(MYLK):c.1516A>G (p.Arg506Gly) rs77323602
NM_053025.4(MYLK):c.1609G>A (p.Val537Ile) rs199988497
NM_053025.4(MYLK):c.1651+6T>A rs820329
NM_053025.4(MYLK):c.1804+8C>T rs820355
NM_053025.4(MYLK):c.1968G>T (p.Trp656Cys) rs138172035
NM_053025.4(MYLK):c.2023G>A (p.Gly675Arg) rs147008323
NM_053025.4(MYLK):c.2101G>A (p.Ala701Thr) rs142835596
NM_053025.4(MYLK):c.2388C>T (p.Leu796=) rs193007255
NM_053025.4(MYLK):c.24C>G (p.Ala8=) rs78118111
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.260G>A (p.Gly87Glu) rs368325180
NM_053025.4(MYLK):c.2628C>T (p.Arg876=) rs571744275
NM_053025.4(MYLK):c.2693G>A (p.Arg898Gln) rs145507832
NM_053025.4(MYLK):c.2742C>A (p.Asp914Glu) rs3732487
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.3242A>G (p.His1081Arg) rs113491038
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.3448+15G>A rs199789942
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.382G>A (p.Ala128Thr) rs147840022
NM_053025.4(MYLK):c.383C>T (p.Ala128Val) rs143896146
NM_053025.4(MYLK):c.3868G>A (p.Glu1290Lys) rs145953933
NM_053025.4(MYLK):c.3987T>G (p.Asp1329Glu) rs9844788
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.411C>G (p.Ser137=) rs55760507
NM_053025.4(MYLK):c.4194C>T (p.His1398=) rs17298941
NM_053025.4(MYLK):c.422+14G>C rs146112057
NM_053025.4(MYLK):c.4289-10dup rs41431347
NM_053025.4(MYLK):c.4289-4C>G rs376670657
NM_053025.4(MYLK):c.4289-9C>G rs41443051
NM_053025.4(MYLK):c.4317T>C (p.Asp1439=) rs1254392
NM_053025.4(MYLK):c.4349G>A (p.Arg1450Gln) rs41366751
NM_053025.4(MYLK):c.439C>T (p.Pro147Ser) rs9840993
NM_053025.4(MYLK):c.4415+9A>G rs187964526
NM_053025.4(MYLK):c.4620-12G>A rs41301337
NM_053025.4(MYLK):c.4620-6C>T rs113607507
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.4842T>C (p.Asn1614=) rs820463
NM_053025.4(MYLK):c.4882G>A (p.Val1628Met) rs76655666
NM_053025.4(MYLK):c.5079G>A (p.Lys1693=) rs141467675
NM_053025.4(MYLK):c.5368+13_5368+21del rs146990616
NM_053025.4(MYLK):c.5441C>T (p.Thr1814Ile) rs142220417
NM_053025.4(MYLK):c.5448C>T (p.Arg1816=) rs56262958
NM_053025.4(MYLK):c.601C>T (p.Leu201=) rs773082759
NM_053025.4(MYLK):c.62C>A (p.Pro21His) rs28497577
NM_053025.4(MYLK):c.652C>T (p.Leu218=) rs113035707
NM_053025.4(MYLK):c.755-12C>T rs138877679
NM_053025.4(MYLK):c.782T>C (p.Val261Ala) rs3796164
NM_053025.4(MYLK):c.984G>A (p.Ser328=) rs115018449
NM_053025.4(MYLK):c.993G>A (p.Thr331=) rs55932343

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