ClinVar Miner

List of variants in gene combination EYA4, TARID reported as likely benign for cardiomyopathy

Included ClinVar conditions (519):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_004100.5(EYA4):c.*3014T>C rs76510133 0.05509
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.*2799C>A rs143596676 0.00882
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.1617-13C>G rs756045097 0.00018
NM_004100.5(EYA4):c.1617-11C>T rs118166702 0.00017
NM_004100.5(EYA4):c.1422G>A (p.Gly474=) rs138141986 0.00011
NM_004100.5(EYA4):c.1338A>G (p.Leu446=) rs200309400 0.00006
NM_004100.5(EYA4):c.1773G>A (p.Arg591=) rs772266373 0.00006
NM_004100.5(EYA4):c.1611C>T (p.Ser537=) rs757995893 0.00004
NM_004100.5(EYA4):c.1437G>A (p.Arg479=) rs142263016 0.00003
NM_004100.5(EYA4):c.1534C>T (p.Leu512=) rs1451874529 0.00003
NM_004100.5(EYA4):c.1653A>G (p.Gln551=) rs747398475 0.00003
NM_004100.5(EYA4):c.1707C>A (p.Pro569=) rs1197553602 0.00003
NM_004100.5(EYA4):c.1341-18G>A rs763846902 0.00002
NM_004100.5(EYA4):c.1506C>T (p.Leu502=) rs753035830 0.00002
NM_004100.5(EYA4):c.1540T>C (p.Leu514=) rs779172500 0.00002
NM_004100.5(EYA4):c.1644G>A (p.Thr548=) rs371913096 0.00002
NM_004100.5(EYA4):c.1739-9A>G rs754524311 0.00002
NM_004100.5(EYA4):c.1308T>C (p.Asp436=) rs1029890565 0.00001
NM_004100.5(EYA4):c.1494C>T (p.Asn498=) rs748934740 0.00001
NM_004100.5(EYA4):c.1617-20A>G rs748106021 0.00001
NM_004100.5(EYA4):c.1635C>T (p.Val545=) rs770537738 0.00001
NM_004100.5(EYA4):c.1671G>A (p.Ala557=) rs768995654 0.00001
NM_004100.5(EYA4):c.1738+16T>C rs1170264132 0.00001
NM_004100.5(EYA4):c.1739-4C>G rs778226541 0.00001
NM_004100.5(EYA4):c.1782A>G (p.Arg594=) rs1309570149 0.00001
NM_004100.5(EYA4):c.1839+18A>G rs1305220868 0.00001
NM_004100.5(EYA4):c.1840-16T>G rs1039495587 0.00001
NM_004100.5(EYA4):c.*2968T>A rs181492427
NM_004100.5(EYA4):c.1282-16C>G
NM_004100.5(EYA4):c.1282-6T>A
NM_004100.5(EYA4):c.1296T>G (p.Val432=) rs1799264613
NM_004100.5(EYA4):c.1340+16_1340+19del
NM_004100.5(EYA4):c.1340+19T>C
NM_004100.5(EYA4):c.1340+20A>G
NM_004100.5(EYA4):c.1341-16A>T
NM_004100.5(EYA4):c.1341-17T>C
NM_004100.5(EYA4):c.1359T>C (p.Thr453=)
NM_004100.5(EYA4):c.1386T>C (p.Ser462=)
NM_004100.5(EYA4):c.1404A>G (p.Pro468=)
NM_004100.5(EYA4):c.1464A>G (p.Val488=)
NM_004100.5(EYA4):c.1502-11T>C rs1260772418
NM_004100.5(EYA4):c.1502-12T>C
NM_004100.5(EYA4):c.1512C>T (p.Gly504=)
NM_004100.5(EYA4):c.1518C>G (p.Ala506=)
NM_004100.5(EYA4):c.1521G>A (p.Lys507=)
NM_004100.5(EYA4):c.1566A>T (p.Thr522=)
NM_004100.5(EYA4):c.1616+14T>A
NM_004100.5(EYA4):c.1616+9A>C rs1799507815
NM_004100.5(EYA4):c.1620T>C (p.Ser540=) rs200224388
NM_004100.5(EYA4):c.1647A>T (p.Thr549=)
NM_004100.5(EYA4):c.1656G>A (p.Leu552=)
NM_004100.5(EYA4):c.1659C>T (p.Ile553=) rs1345813435
NM_004100.5(EYA4):c.1665A>T (p.Ala555=) rs1583560997
NM_004100.5(EYA4):c.1677T>A (p.Val559=) rs2128812082
NM_004100.5(EYA4):c.1680A>C (p.Leu560=) rs535466937
NM_004100.5(EYA4):c.1707C>G (p.Pro569=) rs1197553602
NM_004100.5(EYA4):c.1707C>T (p.Pro569=) rs1197553602
NM_004100.5(EYA4):c.1738+8A>G
NM_004100.5(EYA4):c.1739-20T>G
NM_004100.5(EYA4):c.1779C>G (p.Gly593=)
NM_004100.5(EYA4):c.1791G>A (p.Val597=) rs1583567927
NM_004100.5(EYA4):c.1794T>C (p.Tyr598=) rs1370711989
NM_004100.5(EYA4):c.1800A>G (p.Val600=)
NM_004100.5(EYA4):c.1839+13A>T rs368743262
NM_004100.5(EYA4):c.1840-11T>G
NM_004100.5(EYA4):c.1840-13_1840-11del
NM_004100.5(EYA4):c.1840-14T>G
NM_004100.5(EYA4):c.1896A>G (p.Gln632=)

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