List of variants in gene MYO7A reported by ClinGen Hearing Loss Variant Curation Expert Panel

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.905G>A (p.Arg302His)	rs41298135	0.00281
NM_000260.4(MYO7A):c.1007G>A (p.Arg336His)	rs45629132	0.00164
NM_000260.4(MYO7A):c.19G>A (p.Gly7Arg)	rs372509310	0.00043
NM_000260.4(MYO7A):c.324C>T (p.Tyr108=)	rs116892396	0.00030
NM_000260.4(MYO7A):c.3527G>A (p.Ser1176Asn)	rs373147966	0.00026
NM_000260.4(MYO7A):c.2527G>A (p.Val843Met)	rs140559111	0.00024
NM_000260.4(MYO7A):c.2476G>A (p.Ala826Thr)	rs368341987	0.00021
NM_000260.4(MYO7A):c.1997G>A (p.Arg666Gln)	rs782396605	0.00009
NM_000260.4(MYO7A):c.3862G>C (p.Ala1288Pro)	rs749747871	0.00006
NM_000260.4(MYO7A):c.5618G>A (p.Arg1873Gln)	rs397516322	0.00006
NM_000260.4(MYO7A):c.631A>G (p.Ser211Gly)	rs111033486	0.00005
NM_000260.4(MYO7A):c.3503G>A (p.Arg1168Gln)	rs797044516	0.00004
NM_000260.4(MYO7A):c.6326C>T (p.Thr2109Ile)	rs377670513	0.00004
NM_000260.4(MYO7A):c.401T>A (p.Ile134Asn)	rs111033181	0.00003
NM_000260.4(MYO7A):c.2904G>T (p.Glu968Asp)	rs111033233	0.00002
NM_000260.4(MYO7A):c.3827C>T (p.Ser1276Leu)	rs369458838	0.00002
NM_000260.4(MYO7A):c.1208A>G (p.Tyr403Cys)	rs797044511	0.00001
NM_000260.4(MYO7A):c.2558G>A (p.Arg853His)	rs111033437	0.00001
NM_000260.4(MYO7A):c.3491G>A (p.Arg1164Gln)	rs782350886	0.00001
NM_000260.4(MYO7A):c.5804T>C (p.Leu1935Pro)	rs397516323	0.00001
NM_000260.4(MYO7A):c.1183C>T (p.Arg395Cys)	rs782279338
NM_000260.4(MYO7A):c.1817G>A (p.Arg606His)	rs782311929
NM_000260.4(MYO7A):c.1849T>C (p.Ser617Pro)	rs782063761
NM_000260.4(MYO7A):c.3503+12_3503+33del	rs111033223
NM_000260.4(MYO7A):c.3546C>A (p.Asn1182Lys)	rs1555090294
NM_000260.4(MYO7A):c.4115T>G (p.Val1372Gly)	rs869312181
NM_000260.4(MYO7A):c.6062A>G (p.Lys2021Arg)	rs876657655
NM_000260.4(MYO7A):c.6560G>A (p.Gly2187Asp)	rs397516332
NM_000260.4(MYO7A):c.977T>A (p.Leu326Gln)	rs797044491

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