List of variants reported as uncertain significance for Autosomal dominant nonsyndromic hearing loss 4A; Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001145809.2(MYH14):c.3850C>T (p.Arg1284Trp)	rs201515738	0.00037
NM_001145809.2(MYH14):c.1067C>T (p.Thr356Met)	rs151082668	0.00011
NM_001145809.2(MYH14):c.3304C>T (p.Arg1102Trp)	rs397516629	0.00011
NM_001145809.2(MYH14):c.3821G>A (p.Arg1274Gln)	rs763472009	0.00010
NM_001145809.2(MYH14):c.1631C>T (p.Pro544Leu)	rs371300947	0.00003
NM_001145809.2(MYH14):c.3913C>T (p.Arg1305Cys)	rs755704452	0.00003
NM_001145809.2(MYH14):c.4088G>A (p.Arg1363His)	rs727504915	0.00003
NM_001145809.2(MYH14):c.3141C>T (p.Leu1047=)	rs886054592	0.00001
NM_001145809.2(MYH14):c.3401A>G (p.Gln1134Arg)	rs934260773	0.00001
NM_001145809.2(MYH14):c.5875C>T (p.Arg1959Trp)	rs758424787	0.00001
NM_001145809.2(MYH14):c.2282G>C (p.Gly761Ala)
NM_001145809.2(MYH14):c.2299C>T (p.Arg767Cys)	rs28940307
NM_001145809.2(MYH14):c.5384G>A (p.Arg1795His)	rs567922009

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