ClinVar Miner

List of variants in gene MYO15A reported as uncertain significance by Molecular Diagnosis Center for Deafness

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.9478C>T (p.Leu3160Phe) rs140029076 0.00658
NM_016239.4(MYO15A):c.4777G>A (p.Glu1593Lys) rs376469502 0.00008
NM_016239.4(MYO15A):c.1261C>T (p.Pro421Ser) rs762439635 0.00003
NM_016239.4(MYO15A):c.4642G>A (p.Ala1548Thr) rs201067821 0.00002
NM_016239.4(MYO15A):c.4310A>G (p.Tyr1437Cys) rs749812958 0.00001
NM_016239.4(MYO15A):c.4430G>A (p.Arg1477His) rs374320243 0.00001
NM_016239.4(MYO15A):c.6397A>G (p.Asn2133Asp) rs769491829 0.00001
NM_016239.4(MYO15A):c.10183C>T (p.Leu3395Phe) rs952306971
NM_016239.4(MYO15A):c.2257G>C (p.Ala753Pro) rs776096881
NM_016239.4(MYO15A):c.3926A>T (p.Gln1309Leu) rs777366131
NM_016239.4(MYO15A):c.3971C>A (p.Ala1324Asp) rs1261541284
NM_016239.4(MYO15A):c.4037A>G (p.Lys1346Arg) rs2046141865
NM_016239.4(MYO15A):c.4567C>A (p.Leu1523Met) rs2046256041
NM_016239.4(MYO15A):c.4676T>C (p.Leu1559Ser) rs1391365421
NM_016239.4(MYO15A):c.4784T>C (p.Leu1595Pro) rs1368423304
NM_016239.4(MYO15A):c.4817A>G (p.Asn1606Ser) rs2142323278
NM_016239.4(MYO15A):c.5036G>A (p.Cys1679Tyr) rs2142328201
NM_016239.4(MYO15A):c.5360G>A (p.Arg1787Lys) rs2142335062
NM_016239.4(MYO15A):c.5507T>C (p.Leu1836Pro) rs1253612362
NM_016239.4(MYO15A):c.5557C>G (p.His1853Asp) rs747691685
NM_016239.4(MYO15A):c.6338T>A (p.Ile2113Asn) rs2046471942
NM_016239.4(MYO15A):c.6616T>A (p.Leu2206Ile) rs777487622
NM_016239.4(MYO15A):c.6620C>T (p.Pro2207Leu) rs876657903
NM_016239.4(MYO15A):c.6716A>C (p.His2239Pro) rs760577812
NM_016239.4(MYO15A):c.735C>G (p.Tyr245Ter) rs758073713
NM_016239.4(MYO15A):c.8459G>C (p.Ser2820Thr) rs2142382409
NM_016239.4(MYO15A):c.9532T>C (p.Cys3178Arg) rs2046792650
NM_016239.4(MYO15A):c.9868A>G (p.Met3290Val) rs2142412949

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.