ClinVar Miner

List of variants in gene EYA4, TARID studied for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP
NM_004100.5(EYA4):c.*1264T>A rs9483585
NM_004100.5(EYA4):c.*1346C>T
NM_004100.5(EYA4):c.*1350G>A rs553570769
NM_004100.5(EYA4):c.*1363G>A
NM_004100.5(EYA4):c.*1434A>G rs9483586
NM_004100.5(EYA4):c.*1440C>A
NM_004100.5(EYA4):c.*1484C>T
NM_004100.5(EYA4):c.*1513T>C rs886061092
NM_004100.5(EYA4):c.*1532G>A
NM_004100.5(EYA4):c.*1551G>T
NM_004100.5(EYA4):c.*15C>T
NM_004100.5(EYA4):c.*1600G>A
NM_004100.5(EYA4):c.*1658C>T rs73546865
NM_004100.5(EYA4):c.*1744G>A rs542230437
NM_004100.5(EYA4):c.*1770T>C
NM_004100.5(EYA4):c.*1812G>T rs555600336
NM_004100.5(EYA4):c.*1820A>T
NM_004100.5(EYA4):c.*1867C>T rs17053540
NM_004100.5(EYA4):c.*1905T>A rs542036379
NM_004100.5(EYA4):c.*1943C>T
NM_004100.5(EYA4):c.*2010A>G rs886061093
NM_004100.5(EYA4):c.*2044A>G
NM_004100.5(EYA4):c.*2049T>C
NM_004100.5(EYA4):c.*2108A>G rs17053541
NM_004100.5(EYA4):c.*2184A>T rs17053542
NM_004100.5(EYA4):c.*2188T>A rs376366555
NM_004100.5(EYA4):c.*222G>A
NM_004100.5(EYA4):c.*2269C>T rs533609774
NM_004100.5(EYA4):c.*2302G>A rs41286208
NM_004100.5(EYA4):c.*2359C>T rs547907467
NM_004100.5(EYA4):c.*2360G>A rs886061094
NM_004100.5(EYA4):c.*2377C>T
NM_004100.5(EYA4):c.*23C>T rs3734279
NM_004100.5(EYA4):c.*2439G>A
NM_004100.5(EYA4):c.*2511G>A rs560590444
NM_004100.5(EYA4):c.*2588C>T rs140401218
NM_004100.5(EYA4):c.*265G>A
NM_004100.5(EYA4):c.*2660T>C rs886061096
NM_004100.5(EYA4):c.*2685T>A
NM_004100.5(EYA4):c.*2750C>A rs886061097
NM_004100.5(EYA4):c.*2759G>A rs886061098
NM_004100.5(EYA4):c.*2918G>A
NM_004100.5(EYA4):c.*2968T>A rs181492427
NM_004100.5(EYA4):c.*3014T>C rs76510133
NM_004100.5(EYA4):c.*308G>T
NM_004100.5(EYA4):c.*3121A>G
NM_004100.5(EYA4):c.*3132C>T
NM_004100.5(EYA4):c.*3160C>T
NM_004100.5(EYA4):c.*3211T>G
NM_004100.5(EYA4):c.*3226A>C
NM_004100.5(EYA4):c.*3267C>A rs886061099
NM_004100.5(EYA4):c.*333G>A rs746964933
NM_004100.5(EYA4):c.*347T>C
NM_004100.5(EYA4):c.*379C>A
NM_004100.5(EYA4):c.*566G>T
NM_004100.5(EYA4):c.*633G>A
NM_004100.5(EYA4):c.*726C>A rs55805978
NM_004100.5(EYA4):c.*732A>G
NM_004100.5(EYA4):c.*756A>G
NM_004100.5(EYA4):c.1286G>C (p.Cys429Ser)
NM_004100.5(EYA4):c.1338A>G (p.Leu446=) rs200309400
NM_004100.5(EYA4):c.1347C>G (p.Tyr449Ter) rs1562505728
NM_004100.5(EYA4):c.1418G>T (p.Gly473Val) rs146977269
NM_004100.5(EYA4):c.1463dup (p.Glu490fs)
NM_004100.5(EYA4):c.1617-11C>T rs118166702
NM_004100.5(EYA4):c.1720_1722delTACinsAAA
NM_004100.5(EYA4):c.1739-1G>A rs797045088
NM_004100.5(EYA4):c.1739-64G>A rs143208937
NM_004100.5(EYA4):c.1845C>T (p.Asn615=) rs142721902

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