List of variants in gene MYLK reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 27

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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	0.94358
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	0.53400
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	0.15515
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.3253A>G (p.Thr1085Ala)	rs75370906	0.06202
NM_053025.4(MYLK):c.3027G>A (p.Glu1009=)	rs12172926	0.04612
NM_053025.4(MYLK):c.411C>G (p.Ser137=)	rs55760507	0.03602
NM_053025.4(MYLK):c.3652+11G>A	rs41271437	0.03294
NM_053025.4(MYLK):c.4194C>T (p.His1398=)	rs17298941	0.02481
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.4289-4C>G	rs376670657	0.00156
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.3193GAA[1] (p.Glu1066del)	rs75967604
NM_053025.4(MYLK):c.4289-10dup	rs41431347

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