List of variants in gene MYO7A reported as likely benign for Usher syndrome type 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.6354+35G>A	rs3819170	0.25401
NM_000260.4(MYO7A):c.5156A>G (p.Tyr1719Cys)	rs77625410	0.04825
NM_000260.4(MYO7A):c.4441+89T>C	rs11237115	0.04804
NM_000260.4(MYO7A):c.4023C>T (p.Pro1341=)	rs73495790	0.02130
NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile)	rs35641839	0.01879
NM_000260.4(MYO7A):c.5619G>A (p.Arg1873=)	rs45450893	0.01749
NM_000260.4(MYO7A):c.6519C>T (p.Asn2173=)	rs111033230	0.01207
NM_000260.4(MYO7A):c.*442T>C	rs115238711	0.00963
NM_000260.4(MYO7A):c.3246G>A (p.Thr1082=)	rs35963362	0.00745
NM_000260.4(MYO7A):c.5215C>A (p.Arg1739=)	rs111033477	0.00740
NM_000260.4(MYO7A):c.133-14C>T	rs116228809	0.00719
NM_000260.4(MYO7A):c.*392A>G	rs144527614	0.00712
NM_000260.4(MYO7A):c.4461C>T (p.Asn1487=)	rs56174006	0.00618
NM_000260.4(MYO7A):c.3042G>T (p.Thr1014=)	rs111033507	0.00617
NM_000260.4(MYO7A):c.4074C>T (p.Ser1358=)	rs78996818	0.00559
NM_000260.4(MYO7A):c.4697C>T (p.Thr1566Met)	rs41298747	0.00512
NM_000260.4(MYO7A):c.5835C>T (p.Leu1945=)	rs111033476	0.00408
NM_000260.4(MYO7A):c.5481-14G>A	rs113075052	0.00372
NM_000260.4(MYO7A):c.4698G>A (p.Thr1566=)	rs200207753	0.00295
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.510G>A (p.Leu170=)	rs34477144	0.00138
NM_000260.4(MYO7A):c.4620G>A (p.Ala1540=)	rs41298745	0.00087
NM_000260.4(MYO7A):c.448C>A (p.Arg150=)	rs121965079	0.00031
NM_000260.4(MYO7A):c.324C>T (p.Tyr108=)	rs116892396	0.00030
NM_000260.4(MYO7A):c.3297C>T (p.Pro1099=)	rs367668576	0.00011
NM_000260.4(MYO7A):c.549G>A (p.Ser183=)	rs188198404	0.00009
NM_000260.4(MYO7A):c.397C>A (p.His133Asn)	rs111033403	0.00003
NM_000260.4(MYO7A):c.4619C>T (p.Ala1540Val)	rs111033511	0.00003
NM_000260.4(MYO7A):c.133-7C>T	rs111033221
NM_000260.4(MYO7A):c.2447G>A (p.Arg816His)	rs148343670
NM_000260.4(MYO7A):c.4568+12C>G	rs72933642
NM_000260.4(MYO7A):c.5227C>T (p.Arg1743Trp)	rs111033287
NM_000260.4(MYO7A):c.5598C>A (p.Leu1866=)	rs111033504
NM_000260.4(MYO7A):c.5598C>T (p.Leu1866=)	rs111033504
NM_000260.4(MYO7A):c.93C>T (p.Cys31=)	rs35689081

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