List of variants in gene MYLK reported as likely 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: 39

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HGVS	dbSNP	gnomAD frequency
NM_053025.4(MYLK):c.755-12C>T	rs138877679	0.00212
NM_053025.4(MYLK):c.1007C>T (p.Pro336Leu)	rs35912339	0.00106
NM_053025.4(MYLK):c.3706A>G (p.Met1236Val)	rs113124819	0.00092
NM_053025.4(MYLK):c.3832-6C>T	rs185681684	0.00088
NM_053025.4(MYLK):c.373+18C>T	rs140559450	0.00078
NM_053025.4(MYLK):c.999G>A (p.Pro333=)	rs13319347	0.00045
NM_053025.4(MYLK):c.1991A>G (p.Gln664Arg)	rs200273207	0.00041
NM_053025.4(MYLK):c.3653-10_3653-8del	rs576620371	0.00040
NM_053025.4(MYLK):c.5238+22A>T	rs139889311	0.00034
NM_053025.4(MYLK):c.1609G>A (p.Val537Ile)	rs199988497	0.00026
NM_053025.4(MYLK):c.429A>G (p.Arg143=)	rs149940930	0.00026
NM_053025.4(MYLK):c.5121C>T (p.Arg1707=)	rs144436556	0.00022
NM_053025.4(MYLK):c.3981C>T (p.Val1327=)	rs373556266	0.00017
NM_053025.4(MYLK):c.4293G>A (p.Pro1431=)	rs370153686	0.00016
NM_053025.4(MYLK):c.2023G>A (p.Gly675Arg)	rs147008323	0.00015
NM_053025.4(MYLK):c.2919G>A (p.Pro973=)	rs149482336	0.00014
NM_053025.4(MYLK):c.2589G>A (p.Glu863=)	rs536506601	0.00009
NM_053025.4(MYLK):c.3183C>T (p.Ser1061=)	rs370194660	0.00009
NM_053025.4(MYLK):c.3832-9C>T	rs200022087	0.00008
NM_053025.4(MYLK):c.1651+7T>C	rs758327487	0.00007
NM_053025.4(MYLK):c.382G>A (p.Ala128Thr)	rs147840022	0.00007
NM_053025.4(MYLK):c.3636C>T (p.Pro1212=)	rs780768361	0.00006
NM_053025.4(MYLK):c.3048T>C (p.Asn1016=)	rs758822048	0.00003
NM_053025.4(MYLK):c.4104C>T (p.Ile1368=)	rs376676607	0.00003
NM_053025.4(MYLK):c.609G>A (p.Pro203=)	rs748312013	0.00003
NM_053025.4(MYLK):c.2141-19G>T	rs530951493	0.00002
NM_053025.4(MYLK):c.5155C>T (p.Leu1719=)	rs1057523680	0.00002
NM_053025.4(MYLK):c.771T>C (p.Asn257=)	rs369494886	0.00002
NM_053025.4(MYLK):c.1314C>T (p.Ser438=)	rs200423954	0.00001
NM_053025.4(MYLK):c.2388C>T (p.Leu796=)	rs193007255	0.00001
NM_053025.4(MYLK):c.2853C>T (p.Val951=)	rs769322491	0.00001
NM_053025.4(MYLK):c.3462C>T (p.Ser1154=)	rs768346816	0.00001
NM_053025.4(MYLK):c.4392C>T (p.Tyr1464=)	rs565217509	0.00001
NM_053025.4(MYLK):c.1209C>A (p.Ile403=)	rs1553822281
NM_053025.4(MYLK):c.1713G>A (p.Gln571=)
NM_053025.4(MYLK):c.3138C>T (p.Thr1046=)	rs1279460356
NM_053025.4(MYLK):c.4131G>A (p.Thr1377=)	rs756697460
NM_053025.4(MYLK):c.4344T>C (p.Asp1448=)
NM_053025.4(MYLK):c.588+13_588+16del	rs570821069

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