ClinVar Miner

List of variants in gene MYO3A reported as benign for auditory system disorder

Included ClinVar conditions (325):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_017433.5(MYO3A):c.2716-29G>A rs3818956 0.70675
NM_017433.5(MYO3A):c.1105G>A (p.Val369Ile) rs3817420 0.69434
NM_017433.5(MYO3A):c.1042A>G (p.Ile348Val) rs3824699 0.68769
NM_017433.5(MYO3A):c.3937C>A (p.Arg1313Ser) rs1999240 0.60118
NM_017433.5(MYO3A):c.2867G>A (p.Ser956Asn) rs3758449 0.51636
NM_017433.5(MYO3A):c.1170+7C>T rs3817419 0.47630
NM_017433.5(MYO3A):c.956G>A (p.Arg319His) rs3824700 0.47622
NM_017433.5(MYO3A):c.1104C>T (p.Tyr368=) rs35379457 0.47540
NM_017433.5(MYO3A):c.1053+11C>T rs3824698 0.47508
NM_017433.5(MYO3A):c.1053+12A>G rs3824697 0.47492
NM_017433.5(MYO3A):c.954-32A>G rs3824701 0.47455
NM_017433.5(MYO3A):c.586-22T>C rs3737275 0.43457
NM_017433.5(MYO3A):c.3850A>T (p.Thr1284Ser) rs3740231 0.39847
NM_017433.5(MYO3A):c.3597G>A (p.Glu1199=) rs3740232 0.31670
NM_017433.5(MYO3A):c.3112-4T>C rs16926628 0.12937
NM_017433.5(MYO3A):c.480G>T (p.Thr160=) rs12257119 0.09365
NM_017433.5(MYO3A):c.-15T>A rs11014875 0.08552
NM_017433.5(MYO3A):c.-18G>A rs10128298 0.08551
NM_017433.5(MYO3A):c.624C>T (p.Asp208=) rs35010955 0.08016
NM_017433.5(MYO3A):c.660C>T (p.Ala220=) rs34067308 0.06790
NM_017433.5(MYO3A):c.586-28A>G rs41314631 0.06787
NM_017433.5(MYO3A):c.731+20G>A rs56210104 0.06778
NM_017433.5(MYO3A):c.586-29C>T rs56077277 0.06743
NM_017433.5(MYO3A):c.2497G>T (p.Ala833Ser) rs33947968 0.06209
NM_017433.5(MYO3A):c.4848C>G (p.Ser1616=) rs56316209 0.02444
NM_017433.5(MYO3A):c.533C>T (p.Thr178Ile) rs33968748 0.01220
NM_017433.5(MYO3A):c.3094G>A (p.Ala1032Thr) rs34918608 0.00845
NM_017433.5(MYO3A):c.4465A>G (p.Ile1489Val) rs147376000 0.00541
NM_017433.5(MYO3A):c.949G>C (p.Ala317Pro) rs61731652 0.00334
NM_017433.5(MYO3A):c.4462A>G (p.Lys1488Glu) rs34204285 0.00134
NM_017433.5(MYO3A):c.1242A>T (p.Gly414=) rs3758442 0.00083

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.