ClinVar Miner

List of variants in gene MYLK reported as uncertain significance for not specified

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Total variants: 18
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NM_053025.4(MYLK):c.-4G>A rs989215521
NM_053025.4(MYLK):c.1315G>A (p.Gly439Arg)
NM_053025.4(MYLK):c.1413C>G (p.Tyr471Ter) rs751748077
NM_053025.4(MYLK):c.1609G>A (p.Val537Ile) rs199988497
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.2120A>G (p.Gln707Arg) rs201615936
NM_053025.4(MYLK):c.2338G>C (p.Val780Leu)
NM_053025.4(MYLK):c.2938dup (p.Asp980fs) rs1553803719
NM_053025.4(MYLK):c.3637G>A (p.Val1213Met) rs368390254
NM_053025.4(MYLK):c.3726G>C (p.Gln1242His)
NM_053025.4(MYLK):c.3749G>A (p.Arg1250His) rs139817477
NM_053025.4(MYLK):c.4268C>T (p.Thr1423Met) rs776975714
NM_053025.4(MYLK):c.4882G>A (p.Val1628Met) rs76655666
NM_053025.4(MYLK):c.5412G>T (p.Lys1804Asn) rs139045748
NM_053025.4(MYLK):c.554C>G (p.Thr185Ser) rs1057518439
NM_053025.4(MYLK):c.593A>G (p.Asn198Ser) rs201835018

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