ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 3 by Molecular Diagnosis Center for Deafness

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Total variants: 29
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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.9401G>C (p.Arg3134Pro) rs373695303
NM_016239.4(MYO15A):c.9532T>C (p.Cys3178Arg) rs2046792650
NM_016239.4(MYO15A):c.9868A>G (p.Met3290Val) rs2142412949

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