ClinVar Miner

List of variants in gene EYA4, TARID studied for Autosomal dominant nonsyndromic hearing loss 10

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Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_004100.5(EYA4):c.*1264T>A rs9483585 0.99999
NM_004100.5(EYA4):c.*1434A>G rs9483586 0.79868
NM_004100.5(EYA4):c.*23C>T rs3734279 0.35809
NM_004100.5(EYA4):c.*2108A>G rs17053541 0.24433
NM_004100.5(EYA4):c.*2184A>T rs17053542 0.20492
NM_004100.5(EYA4):c.*726C>A rs55805978 0.20466
NM_004100.5(EYA4):c.*1867C>T rs17053540 0.15248
NM_004100.5(EYA4):c.*3014T>C rs76510133 0.05509
NM_004100.5(EYA4):c.*1658C>T rs73546865 0.04226
NM_004100.5(EYA4):c.*2302G>A rs41286208 0.02535
NM_004100.5(EYA4):c.*2685T>A rs41286210 0.01638
NM_004100.5(EYA4):c.1845C>T (p.Asn615=) rs142721902 0.00854
NM_004100.5(EYA4):c.*1484C>T rs116238383 0.00723
NM_004100.5(EYA4):c.*2918G>A rs75986250 0.00369
NM_004100.5(EYA4):c.*2044A>G rs59167148 0.00365
NM_004100.5(EYA4):c.*2588C>T rs140401218 0.00078
NM_004100.5(EYA4):c.*1744G>A rs542230437 0.00064
NM_004100.5(EYA4):c.*1905T>A rs542036379 0.00060
NM_004100.5(EYA4):c.*1770T>C rs765287346 0.00052
NM_004100.5(EYA4):c.*3211T>G rs140619740 0.00043
NM_004100.5(EYA4):c.*2269C>T rs533609774 0.00041
NM_004100.5(EYA4):c.*2511G>A rs560590444 0.00035
NM_004100.5(EYA4):c.*3226A>C rs73546871 0.00035
NM_004100.5(EYA4):c.*333G>A rs746964933 0.00025
NM_004100.5(EYA4):c.*2377C>T rs1205497819 0.00020
NM_004100.5(EYA4):c.*1350G>A rs553570769 0.00018
NM_004100.5(EYA4):c.1617-11C>T rs118166702 0.00017
NM_004100.5(EYA4):c.*2759G>A rs886061098 0.00014
NM_004100.5(EYA4):c.*308G>T rs999799440 0.00014
NM_004100.5(EYA4):c.1418G>T (p.Gly473Val) rs146977269 0.00014
NM_004100.5(EYA4):c.*379C>A rs1025660001 0.00013
NM_004100.5(EYA4):c.1739-64G>A rs143208937 0.00012
NM_004100.5(EYA4):c.*1600G>A rs998755605 0.00011
NM_004100.5(EYA4):c.*2188T>A rs376366555 0.00011
NM_004100.5(EYA4):c.*3121A>G rs755881972 0.00008
NM_004100.5(EYA4):c.*1363G>A rs539858245 0.00007
NM_004100.5(EYA4):c.*15C>T rs773904240 0.00007
NM_004100.5(EYA4):c.*222G>A rs998303327 0.00007
NM_004100.5(EYA4):c.*1812G>T rs555600336 0.00006
NM_004100.5(EYA4):c.*633G>A rs996978211 0.00006
NM_004100.5(EYA4):c.1338A>G (p.Leu446=) rs200309400 0.00006
NM_004100.5(EYA4):c.*732A>G rs902919934 0.00005
NM_004100.5(EYA4):c.*2049T>C rs752513150 0.00004
NM_004100.5(EYA4):c.*2359C>T rs547907467 0.00004
NM_004100.5(EYA4):c.*2360G>A rs886061094 0.00004
NM_004100.5(EYA4):c.*3267C>A rs886061099 0.00003
NM_004100.5(EYA4):c.*1440C>A rs1251468796 0.00001
NM_004100.5(EYA4):c.*1551G>T rs895041455 0.00001
NM_004100.5(EYA4):c.*1820A>T rs184735364 0.00001
NM_004100.5(EYA4):c.*1943C>T rs150567885 0.00001
NM_004100.5(EYA4):c.*2660T>C rs886061096 0.00001
NM_004100.5(EYA4):c.*1346C>T rs772550313
NM_004100.5(EYA4):c.*1513T>C rs886061092
NM_004100.5(EYA4):c.*1532G>A rs776008831
NM_004100.5(EYA4):c.*2010A>G rs886061093
NM_004100.5(EYA4):c.*2439G>A rs1298238435
NM_004100.5(EYA4):c.*265G>A rs983068379
NM_004100.5(EYA4):c.*2750C>A rs886061097
NM_004100.5(EYA4):c.*2968T>A rs181492427
NM_004100.5(EYA4):c.*3132C>T rs1801031145
NM_004100.5(EYA4):c.*3160C>T rs1801032975
NM_004100.5(EYA4):c.*347T>C rs1434297565
NM_004100.5(EYA4):c.*566G>T rs1800870215
NM_004100.5(EYA4):c.*756A>G rs1800887681
NM_004100.5(EYA4):c.1282-12T>A rs2128781753
NM_004100.5(EYA4):c.1347C>G (p.Tyr449Ter) rs1562505728
NM_004100.5(EYA4):c.1468G>T (p.Glu490Ter) rs1305000119
NM_004100.5(EYA4):c.1486A>T (p.Lys496Ter)
NM_004100.5(EYA4):c.1519A>T (p.Lys507Ter)
NM_004100.5(EYA4):c.1720_1722delTACinsAAA rs1800334076
NM_004100.5(EYA4):c.1739-89_1739-85del rs1293390303
NM_004100.5(EYA4):c.1745_1748del (p.Glu582fs)
NM_004100.5(EYA4):c.1759C>T (p.Arg587Ter) rs1554275988

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