ClinVar Miner

List of variants in gene EYA4 reported as likely benign for Cardiovascular phenotype

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_004100.5(EYA4):c.783G>A (p.Thr261=) rs17854076 0.00136
NM_004100.5(EYA4):c.866C>T (p.Thr289Met) rs41286200 0.00067
NM_004100.5(EYA4):c.768A>G (p.Ser256=) rs147135637 0.00039
NM_004100.5(EYA4):c.979G>A (p.Asp327Asn) rs144415484 0.00037
NM_004100.5(EYA4):c.749C>A (p.Thr250Asn) rs143757415 0.00034
NM_004100.5(EYA4):c.1161C>T (p.Leu387=) rs140472262 0.00009
NM_004100.5(EYA4):c.9C>T (p.Asp3=) rs374322196 0.00009
NM_004100.5(EYA4):c.278-4G>A rs201806127 0.00005
NM_004100.5(EYA4):c.741A>G (p.Pro247=) rs752226573 0.00004
NM_004100.5(EYA4):c.999C>A (p.Ser333=) rs894683876 0.00004
NM_004100.5(EYA4):c.528C>T (p.Ala176=) rs199701258 0.00003
NM_004100.5(EYA4):c.660C>A (p.Leu220=) rs755795461 0.00003
NM_004100.5(EYA4):c.813A>G (p.Pro271=) rs370562413 0.00003
NM_004100.5(EYA4):c.955C>T (p.Leu319=) rs370874438 0.00003
NM_004100.5(EYA4):c.348G>A (p.Ala116=) rs373496105 0.00002
NM_004100.5(EYA4):c.579C>T (p.Tyr193=) rs747954279 0.00002
NM_004100.5(EYA4):c.861A>G (p.Ala287=) rs775461679 0.00002
NM_004100.5(EYA4):c.1095T>C (p.Asp365=) rs779806687 0.00001
NM_004100.5(EYA4):c.213A>C (p.Glu71Asp) rs200042576 0.00001
NM_004100.5(EYA4):c.552A>G (p.Thr184=) rs759974412 0.00001
NM_004100.5(EYA4):c.675G>T (p.Gly225=) rs746266041 0.00001
NM_004100.5(EYA4):c.723A>G (p.Pro241=) rs556550485 0.00001
NM_004100.5(EYA4):c.888G>A (p.Ser296=) rs768010410 0.00001
NM_004100.5(EYA4):c.1053C>T (p.Ser351=)
NM_004100.5(EYA4):c.1068G>A (p.Arg356=)
NM_004100.5(EYA4):c.1152C>T (p.His384=)
NM_004100.5(EYA4):c.1167G>A (p.Gly389=)
NM_004100.5(EYA4):c.12C>T (p.Ser4=)
NM_004100.5(EYA4):c.192T>C (p.Thr64=)
NM_004100.5(EYA4):c.255C>T (p.Cys85=) rs2128626096
NM_004100.5(EYA4):c.315C>T (p.Ser105=)
NM_004100.5(EYA4):c.324C>G (p.Thr108=)
NM_004100.5(EYA4):c.405A>G (p.Ala135=)
NM_004100.5(EYA4):c.468A>T (p.Ala156=)
NM_004100.5(EYA4):c.51A>G (p.Thr17=) rs1038991613
NM_004100.5(EYA4):c.528C>G (p.Ala176=)
NM_004100.5(EYA4):c.540C>T (p.Ala180=)
NM_004100.5(EYA4):c.546A>T (p.Ser182=)
NM_004100.5(EYA4):c.54A>G (p.Glu18=)
NM_004100.5(EYA4):c.630A>G (p.Gln210=)
NM_004100.5(EYA4):c.633T>G (p.Thr211=) rs1794503381
NM_004100.5(EYA4):c.642A>G (p.Pro214=)
NM_004100.5(EYA4):c.768A>C (p.Ser256=)
NM_004100.5(EYA4):c.84-4C>T
NM_004100.5(EYA4):c.867G>A (p.Thr289=) rs763899252
NM_004100.5(EYA4):c.925A>G (p.Thr309Ala) rs556335059
NM_004100.5(EYA4):c.966A>G (p.Gln322=) rs762696698
NM_004100.5(EYA4):c.969A>T (p.Pro323=)
NM_004100.5(EYA4):c.978C>T (p.Phe326=) rs773095472
NM_004100.5(EYA4):c.996C>T (p.Pro332=)

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