List of variants in gene MYH11 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.739C>T (p.Arg247Cys)	rs150759461	0.00174
NM_002474.3(MYH11):c.633+1942T>C	rs199755371	0.00065
NM_002474.3(MYH11):c.2049C>T (p.His683=)	rs150924100	0.00061
NM_002474.3(MYH11):c.12G>A (p.Lys4=)	rs112650390	0.00057
NM_002474.3(MYH11):c.429G>A (p.Lys143=)	rs200672270	0.00056
NM_002474.3(MYH11):c.3031T>C (p.Leu1011=)	rs112861184	0.00053
NM_002474.3(MYH11):c.1732A>G (p.Ile578Val)	rs111936548	0.00052
NM_002474.3(MYH11):c.3816G>A (p.Glu1272=)	rs112990531	0.00046
NM_002474.3(MYH11):c.471C>T (p.Ile157=)	rs140267000	0.00036
NM_002474.3(MYH11):c.914A>G (p.Asn305Ser)	rs185661462	0.00026
NM_002474.3(MYH11):c.3121+19G>A	rs369952802	0.00014
NM_002474.3(MYH11):c.1575+7G>A	rs754750176	0.00004
NM_002474.3(MYH11):c.1402-13G>A	rs201713082	0.00002
NM_002474.3(MYH11):c.684C>T (p.Phe228=)	rs368292089	0.00002
NM_002474.3(MYH11):c.2412-4C>T	rs750313377	0.00001
NM_002474.3(MYH11):c.2997+10G>T	rs886051760	0.00001
NM_002474.3(MYH11):c.3294-10del	rs756946356	0.00001
NM_002474.3(MYH11):c.768C>T (p.Ile256=)	rs756118392	0.00001
NM_002474.3(MYH11):c.1464C>T (p.Asn488=)	rs752601338
NM_002474.3(MYH11):c.2653-19C>T	rs1490690225
NM_002474.3(MYH11):c.3420G>A (p.Gln1140=)	rs972414065
NM_002474.3(MYH11):c.912C>T (p.Phe304=)	rs1060504022

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