List of variants in gene MYLK reported as benign by GeneDx

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: 45

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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.3402C>T (p.Asn1134=)	rs865358	0.94746
NM_053025.4(MYLK):c.1804+8C>T	rs820355	0.91605
NM_053025.4(MYLK):c.439C>T (p.Pro147Ser)	rs9840993	0.88650
NM_053025.4(MYLK):c.1005C>T (p.Thr335=)	rs4678047	0.59203
NM_053025.4(MYLK):c.3558C>T (p.Thr1186=)	rs40305	0.52821
NM_053025.4(MYLK):c.4317T>C (p.Asp1439=)	rs1254392	0.24353
NM_053025.4(MYLK):c.4842T>C (p.Asn1614=)	rs820463	0.21770
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	0.15859
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.3253A>G (p.Thr1085Ala)	rs75370906	0.05750
NM_053025.4(MYLK):c.3027G>A (p.Glu1009=)	rs12172926	0.04612
NM_053025.4(MYLK):c.411C>G (p.Ser137=)	rs55760507	0.03379
NM_053025.4(MYLK):c.3652+11G>A	rs41271437	0.03217
NM_053025.4(MYLK):c.4620-12G>A	rs41301337	0.03066
NM_053025.4(MYLK):c.4194C>T (p.His1398=)	rs17298941	0.02481
NM_053025.4(MYLK):c.2533C>T (p.Arg845Cys)	rs3732485	0.01645
NM_053025.4(MYLK):c.1516+16C>T	rs77590783	0.01444
NM_053025.4(MYLK):c.1327C>T (p.Pro443Ser)	rs35156360	0.01032
NM_053025.4(MYLK):c.383C>T (p.Ala128Val)	rs143896146	0.00758
NM_053025.4(MYLK):c.2101G>A (p.Ala701Thr)	rs142835596	0.00592
NM_053025.4(MYLK):c.3987T>G (p.Asp1329Glu)	rs9844788	0.00558
NM_053025.4(MYLK):c.5368+13_5368+21del	rs146990616	0.00539
NM_053025.4(MYLK):c.4764G>A (p.Pro1588=)	rs56056823	0.00499
NM_053025.4(MYLK):c.652C>T (p.Leu218=)	rs113035707	0.00415
NM_053025.4(MYLK):c.479C>G (p.Pro160Arg)	rs111256888	0.00413
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.3242A>G (p.His1081Arg)	rs113491038	0.00235
NM_053025.4(MYLK):c.755-12C>T	rs138877679	0.00206
NM_053025.4(MYLK):c.5441C>T (p.Thr1814Ile)	rs142220417	0.00190
NM_053025.4(MYLK):c.2388C>T (p.Leu796=)	rs193007255	0.00054
NM_053025.4(MYLK):c.3448+15G>A	rs199789942	0.00050
NM_053025.4(MYLK):c.382G>A (p.Ala128Thr)	rs147840022	0.00042
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.3193GAA[1] (p.Glu1066del)	rs75967604
NM_053025.4(MYLK):c.4289-10dup	rs200371896
NM_053025.4(MYLK):c.4289-9C>G	rs41443051

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