ClinVar Miner

List of variants reported as uncertain significance for Autosomal dominant nonsyndromic hearing loss 10

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Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_004100.5(EYA4):c.*1744G>A rs542230437 0.00064
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.987G>T (p.Met329Ile) rs146144708 0.00021
NM_004100.5(EYA4):c.*2377C>T rs1205497819 0.00020
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.-124C>T rs886061088 0.00010
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.1107+13A>C rs775989680 0.00005
NM_004100.5(EYA4):c.*2049T>C rs752513150 0.00004
NM_004100.5(EYA4):c.*2360G>A rs886061094 0.00004
NM_004100.5(EYA4):c.1223G>A (p.Arg408His) rs760787542 0.00004
NM_004100.5(EYA4):c.182C>T (p.Thr61Ile) rs778473535 0.00004
NM_004100.5(EYA4):c.*3267C>A rs886061099 0.00003
NM_004100.5(EYA4):c.860C>T (p.Ala287Val) rs374522988 0.00003
NM_004100.5(EYA4):c.970+5A>G rs886061089 0.00003
NM_004100.5(EYA4):c.1107+10C>G rs752586864 0.00002
NM_004100.5(EYA4):c.347C>T (p.Ala116Val) rs747223436 0.00002
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.*1943C>T rs150567885 0.00001
NM_004100.5(EYA4):c.*2660T>C rs886061096 0.00001
NM_004100.5(EYA4):c.-256C>T rs886061086 0.00001
NM_004100.5(EYA4):c.438-15T>C rs752763979 0.00001
NM_004100.5(EYA4):c.888G>A (p.Ser296=) rs768010410 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.*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.-408G>T rs886061085
NM_004100.5(EYA4):c.-430T>C rs886061084
NM_004100.5(EYA4):c.1020T>A (p.Asp340Glu)
NM_004100.5(EYA4):c.1181A>G (p.Lys394Arg) rs1796360086
NM_004100.5(EYA4):c.344G>C (p.Gly115Ala) rs1793929707
NM_004100.5(EYA4):c.371-15_371-14insAG
NM_004100.5(EYA4):c.701C>T (p.Thr234Ile)
NM_004100.5(EYA4):c.978C>G (p.Phe326Leu) rs773095472

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