List of variants in gene MYO6 reported as likely benign for auditory system disorder

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: 35

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.1722C>T (p.Asp574=)	rs11756446	0.04242
NM_004999.4(MYO6):c.3303C>T (p.Cys1101=)	rs9443199	0.02151
NM_004999.4(MYO6):c.*1962A>G	rs80199115	0.01750
NM_004999.4(MYO6):c.*3546A>G	rs73751758	0.01688
NM_004999.4(MYO6):c.*1469G>T	rs74367845	0.01285
NM_004999.4(MYO6):c.1176A>G (p.Thr392=)	rs2273857	0.01200
NM_004999.4(MYO6):c.*3509G>A	rs78129547	0.00783
NM_004999.4(MYO6):c.*2910T>A	rs140495245	0.00749
NM_004999.4(MYO6):c.1120T>C (p.Tyr374His)	rs61732664	0.00738
NM_004999.4(MYO6):c.*3288T>C	rs118121148	0.00533
NM_004999.4(MYO6):c.1224-4A>G	rs144031818	0.00238
NM_004999.4(MYO6):c.*4095G>A	rs185154265	0.00151
NM_004999.4(MYO6):c.2517T>C (p.Gly839=)	rs112597191	0.00135
NM_004999.4(MYO6):c.1144G>A (p.Asp382Asn)	rs111530469	0.00134
NM_004999.4(MYO6):c.*303A>G	rs146133231	0.00128
NM_004999.4(MYO6):c.1025C>T (p.Ala342Val)	rs145564837	0.00128
NM_004999.4(MYO6):c.*1232C>T	rs182487428	0.00051
NM_004999.4(MYO6):c.2836C>T (p.Arg946Cys)	rs141845119	0.00039
NM_004999.4(MYO6):c.*3230T>C	rs562815854	0.00038
NM_004999.4(MYO6):c.*3874G>A	rs187631847	0.00032
NM_004999.4(MYO6):c.*4288G>A	rs570588843	0.00029
NM_004999.4(MYO6):c.*1738A>G	rs193019967	0.00028
NM_004999.4(MYO6):c.475G>A (p.Glu159Lys)	rs201507590	0.00026
NM_004999.4(MYO6):c.*4428A>G	rs574549669	0.00024
NM_004999.4(MYO6):c.3483G>A (p.Glu1161=)	rs139174622	0.00024
NM_004999.4(MYO6):c.3176G>C (p.Arg1059Thr)	rs202214380	0.00020
NM_004999.4(MYO6):c.*1889A>G	rs189155544	0.00018
NM_004999.4(MYO6):c.1180G>A (p.Val394Ile)	rs373519764	0.00006
NM_004999.4(MYO6):c.2672C>T (p.Thr891Met)	rs146682372	0.00006
NM_004999.4(MYO6):c.553+10A>G	rs188959117	0.00005
NM_004999.4(MYO6):c.189T>G (p.Cys63Trp)	rs768643110	0.00002
NM_004999.4(MYO6):c.*1528C>T	rs188719640
NM_004999.4(MYO6):c.*186A>G	rs571307356
NM_004999.4(MYO6):c.*3039A>G	rs540365866
NM_004999.4(MYO6):c.*4283A>T	rs7746476

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.