List of variants reported as likely benign for Autosomal dominant nonsyndromic hearing loss 4A

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_001145809.2(MYH14):c.*427T>C	rs190088995	0.00273
NM_001145809.2(MYH14):c.1329+15C>T	rs200176028	0.00224
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=)	rs147447646	0.00206
NM_001145809.2(MYH14):c.*301C>T	rs529409417	0.00203
NM_001145809.2(MYH14):c.*368C>G	rs74582015	0.00192
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn)	rs202225655	0.00134
NM_001145809.2(MYH14):c.4417G>A (p.Val1473Met)	rs112716976	0.00107
NM_001145809.2(MYH14):c.36G>A (p.Lys12=)	rs372741317	0.00098
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val)	rs201337011	0.00093
NM_001145809.2(MYH14):c.1919G>A (p.Arg640Gln)	rs199696801	0.00052
NM_001145809.2(MYH14):c.1115-4C>T	rs142696359	0.00036
NM_001145809.2(MYH14):c.4138-13C>T	rs183327883	0.00034
NM_001145809.2(MYH14):c.3871G>T (p.Val1291Leu)	rs202242879	0.00033
NM_001145809.2(MYH14):c.*86G>A	rs772673014	0.00029
NM_001145809.2(MYH14):c.5599C>T (p.Arg1867Cys)	rs187789045	0.00029
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val)	rs200424400	0.00027
NM_001145809.2(MYH14):c.5850G>A (p.Glu1950=)	rs368708096	0.00025
NM_001145809.2(MYH14):c.2645C>T (p.Ala882Val)	rs202065396	0.00022
NM_001145809.2(MYH14):c.3172-12T>C	rs374486787	0.00013
NM_001145809.2(MYH14):c.*81A>G	rs772326631	0.00010
NM_001145809.2(MYH14):c.2544C>T (p.Ile848=)	rs761170226	0.00009
NM_001145809.2(MYH14):c.5447G>A (p.Arg1816His)	rs201923258	0.00009
NM_001145809.2(MYH14):c.2334C>A (p.Leu778=)	rs190941610	0.00006
NM_001145809.2(MYH14):c.565C>T (p.Arg189Cys)	rs200818171	0.00006
NM_001145809.2(MYH14):c.263G>A (p.Arg88Gln)	rs185910660	0.00004
NM_001145809.2(MYH14):c.4903G>A (p.Glu1635Lys)	rs140157424	0.00003
NM_001145809.2(MYH14):c.3303A>G (p.Leu1101=)	rs543799021	0.00001
NM_001145809.2(MYH14):c.5041G>A (p.Glu1681Lys)	rs556548077
NM_001145809.2(MYH14):c.5384G>T (p.Arg1795Leu)	rs567922009

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