List of variants reported as benign for Autosomal dominant nonsyndromic hearing loss 56

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

Total variants: 49

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002160.4(TNC):c.1616A>G (p.Gln539Arg)	rs1757095	0.92655
NM_002160.4(TNC):c.2951-43T>C	rs2210108	0.78376
NM_002160.4(TNC):c.6022G>C (p.Glu2008Gln)	rs13321	0.70769
NM_002160.4(TNC):c.2131+38T>C	rs1755639	0.56660
NM_002160.4(TNC):c.2248-32C>T	rs2989519	0.49672
NM_002160.4(TNC):c.2039A>G (p.Gln680Arg)	rs1061494	0.48121
NM_002160.4(TNC):c.696A>G (p.Val232=)	rs2992147	0.47668
NM_002160.4(TNC):c.5029A>T (p.Ile1677Leu)	rs2104772	0.47499
NM_002160.4(TNC):c.276G>A (p.Val92=)	rs944510	0.47418
NM_002160.4(TNC):c.1867+31T>A	rs1617917	0.32343
NM_002160.4(TNC):c.4575G>A (p.Thr1525=)	rs17819466	0.09070
NM_002160.4(TNC):c.5341G>A (p.Ala1781Thr)	rs2274750	0.05618
NM_002160.4(TNC):c.2389A>C (p.Arg797=)	rs16932195	0.03252
NM_002160.4(TNC):c.2562C>T (p.Asp854=)	rs61739209	0.02861
NM_002160.4(TNC):c.1813G>A (p.Val605Ile)	rs3827816	0.02047
NM_002160.4(TNC):c.2207A>G (p.Asp736Gly)	rs61735551	0.01740
NM_002160.4(TNC):c.6144G>A (p.Gly2048=)	rs79563958	0.01699
NM_002160.4(TNC):c.3165C>T (p.Ala1055=)	rs3748172	0.01635
NM_002160.4(TNC):c.5193G>A (p.Arg1731=)	rs61265377	0.01588
NM_002160.4(TNC):c.3353G>A (p.Arg1118Gln)	rs61738263	0.01534
NM_002160.4(TNC):c.6006G>A (p.Leu2002=)	rs61736828	0.01478
NM_002160.4(TNC):c.5745C>A (p.Thr1915=)	rs10118726	0.01360
NM_002160.4(TNC):c.781G>A (p.Gly261Ser)	rs61736826	0.01088
NM_002160.4(TNC):c.2620A>G (p.Ile874Val)	rs61737743	0.01031
NM_002160.4(TNC):c.1642G>A (p.Val548Met)	rs61729478	0.00984
NM_002160.4(TNC):c.637G>A (p.Gly213Ser)	rs7020958	0.00643
NM_002160.4(TNC):c.6482A>G (p.Asn2161Ser)	rs75198247	0.00615
NM_002160.4(TNC):c.75C>G (p.Leu25=)	rs62638691	0.00502
NM_002160.4(TNC):c.1342C>G (p.Arg448Gly)	rs145086096	0.00442
NM_002160.4(TNC):c.156C>T (p.His52=)	rs7038329	0.00426
NM_002160.4(TNC):c.96G>A (p.Lys32=)	rs145367019	0.00396
NM_002160.4(TNC):c.1508G>A (p.Arg503Lys)	rs114407480	0.00370
NM_002160.4(TNC):c.1719C>T (p.Cys573=)	rs141544394	0.00318
NM_002160.4(TNC):c.6499G>A (p.Val2167Ile)	rs149752009	0.00299
NM_002160.4(TNC):c.3286G>A (p.Ala1096Thr)	rs138406927	0.00295
NM_002160.4(TNC):c.4740C>T (p.Thr1580=)	rs146504512	0.00277
NM_002160.4(TNC):c.945C>T (p.Cys315=)	rs148465701	0.00214
NM_002160.4(TNC):c.1322A>G (p.Asn441Ser)	rs142220270	0.00173
NM_002160.4(TNC):c.628G>A (p.Gly210Ser)	rs144032672	0.00159
NM_002160.4(TNC):c.61G>A (p.Glu21Lys)	rs141126037	0.00125
NM_002160.4(TNC):c.3711G>A (p.Gly1237=)	rs139931208	0.00115
NM_002160.4(TNC):c.2490C>T (p.Ile830=)	rs145321605	0.00102
NM_002160.4(TNC):c.5223G>A (p.Arg1741=)	rs62638694	0.00098
NM_002160.4(TNC):c.2120G>C (p.Arg707Thr)	rs146640511	0.00016
NM_002160.4(TNC):c.2049G>A (p.Glu683=)	rs2274836
NM_002160.4(TNC):c.3375C>A (p.Ser1125Arg)	rs61737056
NM_002160.4(TNC):c.5093G>A (p.Arg1698Gln)	rs61734387
NM_002160.4(TNC):c.5093G>C (p.Arg1698Pro)	rs61734387
NM_002160.4(TNC):c.6099C>T (p.Arg2033=)	rs58547879

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.