List of variants in gene MYH11 reported as likely benign by Illumina Laboratory Services, Illumina

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.387A>G (p.Lys129=)	rs78754138	0.01024
NM_002474.3(MYH11):c.1419G>A (p.Gln473=)	rs61734198	0.00535
NM_002474.3(MYH11):c.453G>A (p.Pro151=)	rs61734199	0.00242
NM_002474.3(MYH11):c.3828G>A (p.Ala1276=)	rs113154524	0.00240
NM_002474.3(MYH11):c.3652-6C>T	rs193922630	0.00219
NM_002474.3(MYH11):c.739C>T (p.Arg247Cys)	rs150759461	0.00174
NM_002474.3(MYH11):c.1848C>T (p.Ala616=)	rs112834652	0.00172
NM_002474.3(MYH11):c.291C>T (p.Asn97=)	rs113363750	0.00106
NM_002474.3(MYH11):c.-67C>T	rs370680984	0.00036
NM_002474.3(MYH11):c.914A>G (p.Asn305Ser)	rs185661462	0.00026
NM_002474.3(MYH11):c.3531G>A (p.Thr1177=)	rs149980738	0.00017
MYH11:c.503-14_503-12del	rs141564071
NM_001040113.1(MYH11):c.-115delG	rs3215003

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.