ClinVar Miner

List of variants in gene MYLK reported as benign by Ambry Genetics

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Gene type:
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Total variants: 32
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HGVS dbSNP
NM_053025.3(MYLK):c.1005C>T (p.Thr335=) rs4678047
NM_053025.3(MYLK):c.1327C>T (p.Pro443Ser) rs35156360
NM_053025.3(MYLK):c.1486C>G (p.Leu496Val) rs9833275
NM_053025.3(MYLK):c.1516A>G (p.Arg506Gly) rs77323602
NM_053025.3(MYLK):c.2023G>A (p.Gly675Arg) rs147008323
NM_053025.3(MYLK):c.2101G>A (p.Ala701Thr) rs142835596
NM_053025.3(MYLK):c.2533C>T (p.Arg845Cys) rs3732485
NM_053025.3(MYLK):c.2582T>C (p.Leu861Pro) rs3732486
NM_053025.3(MYLK):c.2742C>A (p.Asp914Glu) rs3732487
NM_053025.3(MYLK):c.3027G>A (p.Glu1009=) rs12172926
NM_053025.3(MYLK):c.3196_3198delGAA (p.Glu1066del) rs75967604
NM_053025.3(MYLK):c.3253A>G (p.Thr1085Ala) rs75370906
NM_053025.3(MYLK):c.3402C>T (p.Asn1134=) rs865358
NM_053025.3(MYLK):c.3558C>T (p.Thr1186=) rs40305
NM_053025.3(MYLK):c.382G>A (p.Ala128Thr) rs147840022
NM_053025.3(MYLK):c.383C>T (p.Ala128Val) rs143896146
NM_053025.3(MYLK):c.3868G>A (p.Glu1290Lys) rs145953933
NM_053025.3(MYLK):c.3987T>G (p.Asp1329Glu) rs9844788
NM_053025.3(MYLK):c.411C>G (p.Ser137=) rs55760507
NM_053025.3(MYLK):c.4194C>T (p.His1398=) rs17298941
NM_053025.3(MYLK):c.4289-3dupC rs41431347
NM_053025.3(MYLK):c.4317T>C (p.Asp1439=) rs1254392
NM_053025.3(MYLK):c.4349G>A (p.Arg1450Gln) rs41366751
NM_053025.3(MYLK):c.439C>T (p.Pro147Ser) rs9840993
NM_053025.3(MYLK):c.479C>G (p.Pro160Arg) rs111256888
NM_053025.3(MYLK):c.4842T>C (p.Asn1614=) rs820463
NM_053025.3(MYLK):c.5079G>A (p.Lys1693=) rs141467675
NM_053025.3(MYLK):c.5441C>T (p.Thr1814Ile) rs142220417
NM_053025.3(MYLK):c.62C>A (p.Pro21His) rs28497577
NM_053025.3(MYLK):c.652C>T (p.Leu218=) rs113035707
NM_053025.3(MYLK):c.782T>C (p.Val261Ala) rs3796164
NM_053025.3(MYLK):c.984G>A (p.Ser328=) rs115018449

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