List of variants in gene MYLK reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_053025.4(MYLK):c.1486C>G (p.Leu496Val)	rs9833275	0.99852
NM_053025.4(MYLK):c.439C>T (p.Pro147Ser)	rs9840993	0.88650
NM_053025.4(MYLK):c.*1809A>G	rs6438804	0.30158
NM_053025.4(MYLK):c.1651+6T>A	rs820329	0.17955
NM_053025.4(MYLK):c.62C>A (p.Pro21His)	rs28497577	0.17349
NM_053025.4(MYLK):c.782T>C (p.Val261Ala)	rs3796164	0.15515
NM_053025.4(MYLK):c.3253A>G (p.Thr1085Ala)	rs75370906	0.06202
NM_053025.4(MYLK):c.3027G>A (p.Glu1009=)	rs12172926	0.04612
NM_053025.4(MYLK):c.4194C>T (p.His1398=)	rs17298941	0.02481
NM_053025.4(MYLK):c.1516+16C>T	rs77590783	0.01553
NM_053025.4(MYLK):c.2533C>T (p.Arg845Cys)	rs3732485	0.01370
NM_053025.4(MYLK):c.1327C>T (p.Pro443Ser)	rs35156360	0.01032
NM_053025.4(MYLK):c.383C>T (p.Ala128Val)	rs143896146	0.00747
NM_053025.4(MYLK):c.2101G>A (p.Ala701Thr)	rs142835596	0.00637
NM_053025.4(MYLK):c.3987T>G (p.Asp1329Glu)	rs9844788	0.00558
NM_053025.4(MYLK):c.5368+13_5368+21del	rs146990616	0.00551
NM_053025.4(MYLK):c.4764G>A (p.Pro1588=)	rs56056823	0.00499
NM_053025.4(MYLK):c.652C>T (p.Leu218=)	rs113035707	0.00441
NM_053025.4(MYLK):c.479C>G (p.Pro160Arg)	rs111256888	0.00440
NM_053025.4(MYLK):c.4349G>A (p.Arg1450Gln)	rs41366751	0.00406
NM_053025.4(MYLK):c.1516A>G (p.Arg506Gly)	rs77323602	0.00404
NM_053025.4(MYLK):c.422+14G>C	rs146112057	0.00400
NM_053025.4(MYLK):c.984G>A (p.Ser328=)	rs115018449	0.00277
NM_053025.4(MYLK):c.24C>G (p.Ala8=)	rs78118111	0.00229
NM_053025.4(MYLK):c.4620-6C>T	rs113607507	0.00195
NM_053025.4(MYLK):c.399G>T (p.Gln133His)	rs140148380	0.00167
NM_053025.4(MYLK):c.4620-18G>A	rs41305835	0.00153
NM_053025.4(MYLK):c.5448C>T (p.Arg1816=)	rs56262958	0.00032
NM_053025.4(MYLK):c.3525C>T (p.Asp1175=)	rs147735490	0.00020
NM_053025.4(MYLK):c.3075C>T (p.Pro1025=)	rs144885184	0.00016
NM_053025.4(MYLK):c.3448+15G>A	rs199789942	0.00014
NM_053025.4(MYLK):c.-72C>T	rs2700352
NM_053025.4(MYLK):c.1968G>T (p.Trp656Cys)	rs138172035
NM_053025.4(MYLK):c.260G>A (p.Gly87Glu)	rs368325180
NM_053025.4(MYLK):c.4289-10dup	rs41431347
NM_053025.4(MYLK):c.774-18A>C	rs761133062

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