ClinVar Miner

List of variants in gene EYA1 reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP
NM_000503.6(EYA1):c.*1126T>C
NM_000503.6(EYA1):c.*1135_*1138dup rs886063085
NM_000503.6(EYA1):c.*117G>A rs886063087
NM_000503.6(EYA1):c.*1229G>A
NM_000503.6(EYA1):c.*1275G>A rs192113669
NM_000503.6(EYA1):c.*1284C>A
NM_000503.6(EYA1):c.*1297A>G
NM_000503.6(EYA1):c.*1372_*1375dup rs142792208
NM_000503.6(EYA1):c.*1391G>A
NM_000503.6(EYA1):c.*1529C>T
NM_000503.6(EYA1):c.*1543T>G
NM_000503.6(EYA1):c.*1561A>G
NM_000503.6(EYA1):c.*1598A>C rs886063084
NM_000503.6(EYA1):c.*1672T>A rs777991930
NM_000503.6(EYA1):c.*429T>C
NM_000503.6(EYA1):c.*442G>A rs767388665
NM_000503.6(EYA1):c.*451C>T
NM_000503.6(EYA1):c.*545C>T rs886063086
NM_000503.6(EYA1):c.*70G>A
NM_000503.6(EYA1):c.*755A>T
NM_000503.6(EYA1):c.*770_*773dup rs371488223
NM_000503.6(EYA1):c.*848G>A rs775498240
NM_000503.6(EYA1):c.*866C>T
NM_000503.6(EYA1):c.*86C>A rs186838732
NM_000503.6(EYA1):c.*901dup rs570995924
NM_000503.6(EYA1):c.-155G>A rs886063090
NM_000503.6(EYA1):c.-173G>T rs886063091
NM_000503.6(EYA1):c.-188C>T
NM_000503.6(EYA1):c.-192G>A rs886063092
NM_000503.6(EYA1):c.-242T>G rs886063093
NM_000503.6(EYA1):c.-263C>T rs146081509
NM_000503.6(EYA1):c.-326G>T rs551597748
NM_000503.6(EYA1):c.-340G>C
NM_000503.6(EYA1):c.-429G>A rs886063094
NM_000503.6(EYA1):c.-454G>A rs569684779
NM_000503.6(EYA1):c.-49A>G rs773963094
NM_000503.6(EYA1):c.-75G>C rs558296770
NM_000503.6(EYA1):c.1140+4_1140+7del rs1554605968
NM_000503.6(EYA1):c.1140+5G>A
NM_000503.6(EYA1):c.1258T>C (p.Leu420=) rs200074362
NM_000503.6(EYA1):c.1313A>T (p.Tyr438Phe)
NM_000503.6(EYA1):c.1474C>T (p.Arg492Trp)
NM_000503.6(EYA1):c.1509T>C (p.Thr503=)
NM_000503.6(EYA1):c.1523C>T (p.Ala508Val) rs754901033
NM_000503.6(EYA1):c.1609T>C (p.Cys537Arg) rs1554594182
NM_000503.6(EYA1):c.164C>T (p.Thr55Met) rs201434219
NM_000503.6(EYA1):c.1654GTT[1] (p.Val553del) rs1563621870
NM_000503.6(EYA1):c.1698+14G>A
NM_000503.6(EYA1):c.196G>T (p.Gly66Cys) rs886063089
NM_000503.6(EYA1):c.203-15G>T rs772006212
NM_000503.6(EYA1):c.299C>A (p.Thr100Asn) rs373501480
NM_000503.6(EYA1):c.340T>C (p.Phe114Leu)
NM_000503.6(EYA1):c.378G>A (p.Thr126=)
NM_000503.6(EYA1):c.398C>T (p.Pro133Leu)
NM_000503.6(EYA1):c.403G>A (p.Gly135Ser) rs747476629
NM_000503.6(EYA1):c.415T>C (p.Tyr139His) rs763614581
NM_000503.6(EYA1):c.418+3G>C rs1554550269
NM_000503.6(EYA1):c.556+5G>C rs886063088
NM_000503.6(EYA1):c.671G>T (p.Gly224Val) rs201509408
NM_000503.6(EYA1):c.827-8T>A
NM_000503.6(EYA1):c.865G>T (p.Asp289Tyr) rs201504674
NM_000503.6(EYA1):c.988G>T (p.Asp330Tyr) rs1586100993
NM_172059.5(EYA1):c.34-5589A>G rs886063095
NM_172059.5(EYA1):c.34-5644_34-5643del rs886063096
NM_172059.5(EYA1):c.34-5646_34-5645del rs35320129
NM_172059.5(EYA1):c.34-5669_34-5668dup rs35320129
NM_172059.5(EYA1):c.34-5670C>A rs886063099
NM_172059.5(EYA1):c.34-5671C>A rs886063100

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