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

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Total variants: 30

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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_002700.3(POU4F3):c.325C>T (p.His109Tyr)	rs754773365
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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