ClinVar Miner

List of variants studied for autosomal dominant nonsyndromic hearing loss 56

Included ClinVar conditions (1):
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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_002160.4(TNC):c.1616A>G (p.Gln539Arg) rs1757095 0.92370
NM_002160.4(TNC):c.2951-43T>C rs2210108 0.79228
NM_002160.4(TNC):c.6022G>C (p.Glu2008Gln) rs13321 0.71355
NM_002160.4(TNC):c.2131+38T>C rs1755639 0.56997
NM_002160.4(TNC):c.2248-32C>T rs2989519 0.50397
NM_002160.4(TNC):c.696A>G (p.Val232=) rs2992147 0.48200
NM_002160.4(TNC):c.2039A>G (p.Gln680Arg) rs1061494 0.48121
NM_002160.4(TNC):c.276G>A (p.Val92=) rs944510 0.47973
NM_002160.4(TNC):c.5029A>T (p.Ile1677Leu) rs2104772 0.47499
NM_002160.4(TNC):c.1867+31T>A rs1617917 0.32336
NM_002160.4(TNC):c.4575G>A (p.Thr1525=) rs17819466 0.09039
NM_002160.4(TNC):c.5341G>A (p.Ala1781Thr) rs2274750 0.05620
NM_002160.4(TNC):c.2389A>C (p.Arg797=) rs16932195 0.03496
NM_002160.4(TNC):c.2562C>T (p.Asp854=) rs61739209 0.02872
NM_002160.4(TNC):c.1813G>A (p.Val605Ile) rs3827816 0.02047
NM_002160.4(TNC):c.2207A>G (p.Asp736Gly) rs61735551 0.01898
NM_002160.4(TNC):c.5193G>A (p.Arg1731=) rs61265377 0.01721
NM_002160.4(TNC):c.6006G>A (p.Leu2002=) rs61736828 0.01597
NM_002160.4(TNC):c.3353G>A (p.Arg1118Gln) rs61738263 0.01534
NM_002160.4(TNC):c.6144G>A (p.Gly2048=) rs79563958 0.01419
NM_002160.4(TNC):c.5745C>A (p.Thr1915=) rs10118726 0.01360
NM_002160.4(TNC):c.3165C>T (p.Ala1055=) rs3748172 0.01315
NM_002160.4(TNC):c.2620A>G (p.Ile874Val) rs61737743 0.01101
NM_002160.4(TNC):c.781G>A (p.Gly261Ser) rs61736826 0.01088
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 0.00531
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 0.00393
NM_002160.4(TNC):c.1719C>T (p.Cys573=) rs141544394 0.00347
NM_002160.4(TNC):c.3286G>A (p.Ala1096Thr) rs138406927 0.00324
NM_002160.4(TNC):c.6499G>A (p.Val2167Ile) rs149752009 0.00299
NM_002160.4(TNC):c.4740C>T (p.Thr1580=) rs146504512 0.00277
NM_002160.4(TNC):c.945C>T (p.Cys315=) rs148465701 0.00226
NM_002160.4(TNC):c.1322A>G (p.Asn441Ser) rs142220270 0.00174
NM_002160.4(TNC):c.628G>A (p.Gly210Ser) rs144032672 0.00159
NM_002160.4(TNC):c.2374G>T (p.Gly792Cys) rs150868783 0.00131
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.5317G>A (p.Val1773Met) rs137933052 0.00025
NM_002160.4(TNC):c.6494A>G (p.Gln2165Arg) rs200330029 0.00021
NM_002160.4(TNC):c.2120G>C (p.Arg707Thr) rs146640511 0.00016
NM_002160.4(TNC):c.2239C>T (p.Arg747Trp) rs776411890 0.00007
NM_002160.4(TNC):c.2960C>T (p.Thr987Met) rs778506429 0.00007
NM_002160.4(TNC):c.1580G>C (p.Cys527Ser) rs746843738 0.00001
NM_002160.4(TNC):c.2340G>T (p.Glu780Asp) rs201169030 0.00001
NM_002160.4(TNC):c.1004G>C (p.Gly335Ala)
NM_002160.4(TNC):c.1622G>A (p.Arg541His)
NM_002160.4(TNC):c.2049G>A (p.Glu683=) rs2274836
NM_002160.4(TNC):c.2192A>C (p.Glu731Ala)
NM_002160.4(TNC):c.2434A>G (p.Lys812Glu)
NM_002160.4(TNC):c.2795G>C (p.Gly932Ala) rs766474182
NM_002160.4(TNC):c.3375C>A (p.Ser1125Arg) rs61737056
NM_002160.4(TNC):c.4490G>C (p.Gly1497Ala)
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.5247A>T (p.Gly1749=)
NM_002160.4(TNC):c.5386A>T (p.Thr1796Ser) rs431905513
NM_002160.4(TNC):c.5692G>A (p.Val1898Ile)
NM_002160.4(TNC):c.6099C>T (p.Arg2033=) rs58547879
NM_002160.4(TNC):c.6496-18del rs1419724369
NM_002160.4(TNC):c.6527A>G (p.Glu2176Gly)
NM_002160.4(TNC):c.890A>G (p.Asn297Ser) rs1554717312
Single allele

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