List of variants in gene MYO7A reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 46

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.4461C>T (p.Asn1487=)	rs56174006	0.00618
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.5866G>A (p.Val1956Ile)	rs142293185	0.00386
NM_000260.4(MYO7A):c.1605C>T (p.Asn535=)	rs111033228	0.00336
NM_000260.4(MYO7A):c.905G>A (p.Arg302His)	rs41298135	0.00281
NM_000260.4(MYO7A):c.1854G>A (p.Leu618=)	rs35429535	0.00276
NM_000260.4(MYO7A):c.1554+8G>A	rs111033227	0.00249
NM_000260.4(MYO7A):c.3750+9G>A	rs111033252	0.00197
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.2886G>C (p.Gln962His)	rs200641606	0.00073
NM_000260.4(MYO7A):c.5904C>T (p.His1968=)	rs41298753	0.00072
NM_000260.4(MYO7A):c.4668G>A (p.Pro1556=)	rs376892582	0.00058
NM_000260.4(MYO7A):c.486C>T (p.Ala162=)	rs367687624	0.00051
NM_000260.4(MYO7A):c.5559C>T (p.His1853=)	rs373612656	0.00049
NM_000260.4(MYO7A):c.687C>T (p.Gly229=)	rs371142158	0.00034
NM_000260.4(MYO7A):c.4281G>A (p.Thr1427=)	rs185607254	0.00032
NM_000260.4(MYO7A):c.5253G>T (p.Pro1751=)	rs377388669	0.00032
NM_000260.4(MYO7A):c.448C>A (p.Arg150=)	rs121965079	0.00031
NM_000260.4(MYO7A):c.6165C>T (p.Ser2055=)	rs397516327	0.00029
NM_000260.4(MYO7A):c.2181T>C (p.Phe727=)	rs373656667	0.00028
NM_000260.4(MYO7A):c.2475C>T (p.Arg825=)	rs782711428	0.00011
NM_000260.4(MYO7A):c.3297C>T (p.Pro1099=)	rs367668576	0.00011
NM_000260.4(MYO7A):c.6552G>A (p.Thr2184=)	rs370866578	0.00011
NM_000260.4(MYO7A):c.3987C>T (p.Tyr1329=)	rs560284703	0.00009
NM_000260.4(MYO7A):c.4728G>A (p.Lys1576=)	rs758921557	0.00009
NM_000260.4(MYO7A):c.4920C>T (p.Gly1640=)	rs372882699	0.00009
NM_000260.4(MYO7A):c.549G>A (p.Ser183=)	rs188198404	0.00009
NM_000260.4(MYO7A):c.3651C>T (p.His1217=)	rs776731918	0.00008
NM_000260.4(MYO7A):c.1221C>T (p.Phe407=)	rs782131912	0.00005
NM_000260.4(MYO7A):c.2307C>T (p.Asn769=)	rs782329400	0.00004
NM_000260.4(MYO7A):c.5466C>T (p.Thr1822=)	rs548620787	0.00004
NM_000260.4(MYO7A):c.5004C>T (p.Tyr1668=)	rs1479835169	0.00002
NM_000260.4(MYO7A):c.2122A>G (p.Met708Val)	rs397516293	0.00001
NM_000260.4(MYO7A):c.5928T>G (p.Ala1976=)	rs375155751	0.00001
NM_000260.4(MYO7A):c.939C>T (p.Thr313=)	rs782157346	0.00001
NM_000260.4(MYO7A):c.133-7C>T	rs111033221
NM_000260.4(MYO7A):c.2082G>A (p.Pro694=)	rs782034714
NM_000260.4(MYO7A):c.4167T>G (p.Ala1389=)
NM_000260.4(MYO7A):c.4875C>T (p.Leu1625=)
NM_000260.4(MYO7A):c.5227C>T (p.Arg1743Trp)	rs111033287
NM_000260.4(MYO7A):c.5487C>T (p.Ser1829=)	rs397516318
NM_000260.4(MYO7A):c.5598C>A (p.Leu1866=)	rs111033504
NM_000260.4(MYO7A):c.5727T>G (p.Pro1909=)
NM_000260.4(MYO7A):c.783T>A (p.Gly261=)	rs762667

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