List of variants in gene MYLK reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 57

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HGVS	dbSNP	gnomAD frequency
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.2582T>C (p.Leu861Pro)	rs3732486	0.11664
NM_053025.4(MYLK):c.2742C>A (p.Asp914Glu)	rs3732487	0.06754
NM_053025.4(MYLK):c.2101G>A (p.Ala701Thr)	rs142835596	0.00637
NM_053025.4(MYLK):c.399G>T (p.Gln133His)	rs140148380	0.00167
NM_053025.4(MYLK):c.1132C>G (p.Arg378Gly)	rs11920433	0.00111
NM_053025.4(MYLK):c.3706A>G (p.Met1236Val)	rs113124819	0.00092
NM_053025.4(MYLK):c.1474G>A (p.Ala492Thr)	rs143010767	0.00048
NM_053025.4(MYLK):c.1991A>G (p.Gln664Arg)	rs200273207	0.00041
NM_053025.4(MYLK):c.4348C>T (p.Arg1450Trp)	rs143258617	0.00035
NM_053025.4(MYLK):c.5302A>G (p.Ser1768Gly)	rs149866482	0.00032
NM_053025.4(MYLK):c.2485G>A (p.Glu829Lys)	rs370190691	0.00029
NM_053025.4(MYLK):c.4184T>C (p.Leu1395Pro)	rs146576868	0.00023
NM_053025.4(MYLK):c.4322-11G>A	rs371724615	0.00022
NM_053025.4(MYLK):c.5477C>T (p.Ala1826Val)	rs147187907	0.00022
NM_053025.4(MYLK):c.455G>A (p.Arg152His)	rs201754358	0.00020
NM_053025.4(MYLK):c.257G>A (p.Arg86Gln)	rs138265409	0.00019
NM_053025.4(MYLK):c.2023G>A (p.Gly675Arg)	rs147008323	0.00015
NM_053025.4(MYLK):c.2629G>A (p.Val877Met)	rs34542174	0.00013
NM_053025.4(MYLK):c.5535T>C (p.Asp1845=)	rs748934365	0.00013
NM_053025.4(MYLK):c.2474C>T (p.Pro825Leu)	rs201332554	0.00012
NM_053025.4(MYLK):c.1689C>T (p.Ala563=)	rs760193913	0.00008
NM_053025.4(MYLK):c.2598C>T (p.Gly866=)	rs144654396	0.00008
NM_053025.4(MYLK):c.3696G>A (p.Pro1232=)	rs769086535	0.00008
NM_053025.4(MYLK):c.382G>A (p.Ala128Thr)	rs147840022	0.00007
NM_053025.4(MYLK):c.4332G>A (p.Glu1444=)	rs139884214	0.00007
NM_053025.4(MYLK):c.1167G>A (p.Leu389=)	rs377631029	0.00006
NM_053025.4(MYLK):c.1752A>G (p.Leu584=)	rs775877814	0.00006
NM_053025.4(MYLK):c.1954C>G (p.Pro652Ala)	rs750686734	0.00006
NM_053025.4(MYLK):c.3210C>T (p.Asp1070=)	rs200758888	0.00006
NM_053025.4(MYLK):c.774-15C>G	rs371552521	0.00006
NM_053025.4(MYLK):c.4292C>T (p.Pro1431Leu)	rs746690413	0.00005
NM_053025.4(MYLK):c.2936C>T (p.Pro979Leu)	rs368229473	0.00004
NM_053025.4(MYLK):c.2113C>T (p.Arg705Cys)	rs547322504	0.00003
NM_053025.4(MYLK):c.344G>A (p.Arg115His)	rs141131535	0.00003
NM_053025.4(MYLK):c.4224C>T (p.Asn1408=)	rs149002594	0.00003
NM_053025.4(MYLK):c.2835G>A (p.Val945=)	rs773308800	0.00002
NM_053025.4(MYLK):c.348G>A (p.Gln116=)	rs1275647065	0.00002
NM_053025.4(MYLK):c.3528T>C (p.Ala1176=)	rs766180911	0.00002
NM_053025.4(MYLK):c.435A>C (p.Ser145=)	rs747805468	0.00002
NM_053025.4(MYLK):c.4812C>T (p.Ile1604=)	rs138822291	0.00002
NM_053025.4(MYLK):c.717G>A (p.Ser239=)	rs146960026	0.00002
NM_053025.4(MYLK):c.2227G>A (p.Ala743Thr)	rs145191000	0.00001
NM_053025.4(MYLK):c.3867C>T (p.Ser1289=)	rs561502268	0.00001
NM_053025.4(MYLK):c.4392C>T (p.Tyr1464=)	rs565217509	0.00001
NM_053025.4(MYLK):c.4416-14C>T	rs1392123047	0.00001
NM_053025.4(MYLK):c.4700G>A (p.Arg1567Gln)	rs757766496	0.00001
NM_053025.4(MYLK):c.593A>G (p.Asn198Ser)	rs201835018	0.00001
NM_053025.4(MYLK):c.1179TGT[1] (p.Val395del)	rs771815695
NM_053025.4(MYLK):c.1968G>T (p.Trp656Cys)	rs138172035
NM_053025.4(MYLK):c.2462+20G>A	rs565230903
NM_053025.4(MYLK):c.2829G>A (p.Arg943=)
NM_053025.4(MYLK):c.3193GAA[1] (p.Glu1066del)	rs75967604
NM_053025.4(MYLK):c.4644G>A (p.Glu1548=)
NM_053025.4(MYLK):c.5697G>A (p.Val1899=)	rs2107807094
NM_053031.4(MYLK):c.89-2_89del	rs749876595

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