ClinVar Miner

List of variants in gene EYA1 reported as benign for not provided

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_000503.6(EYA1):c.639+39T>G rs3779747 0.39091
NM_000503.6(EYA1):c.1755T>C (p.His585=) rs10103397 0.35033
NM_000503.6(EYA1):c.1699-23A>G rs10090382 0.34966
NM_000503.6(EYA1):c.1699-84C>G rs10103852 0.34874
NM_000503.6(EYA1):c.1597+59C>T rs7846086 0.30943
NM_000503.6(EYA1):c.1476-21G>T rs3735935 0.30839
NM_000503.6(EYA1):c.1360+53C>T rs4737312 0.29944
NM_000503.6(EYA1):c.-4-297T>C rs1838621 0.27665
NM_000503.6(EYA1):c.418+225T>C rs7008755 0.26477
NM_000503.6(EYA1):c.1050+113G>A rs2053664 0.26106
NM_000503.6(EYA1):c.1699-55G>A rs10103644 0.20964
NM_000503.6(EYA1):c.1278C>T (p.Gly426=) rs4738118 0.13734
NM_000503.6(EYA1):c.1597+60G>A rs79867447 0.12646
NM_000503.6(EYA1):c.125-169T>C rs7840881 0.11230
NM_000503.6(EYA1):c.557-226T>C rs9657098 0.10496
NM_000503.6(EYA1):c.1050+107A>G rs76660214 0.09160
NM_000503.6(EYA1):c.813A>G (p.Thr271=) rs1445398 0.08547
NM_000503.6(EYA1):c.125-258A>G rs7824978 0.08465
NM_000503.6(EYA1):c.826+244C>G rs13278037 0.06965
NM_000503.6(EYA1):c.58C>G (p.Pro20Ala) rs1445404 0.05809
NM_000503.6(EYA1):c.1698+133A>G rs76599768 0.03939
NM_000503.6(EYA1):c.1698+344C>T rs79178549 0.03606
NM_000503.6(EYA1):c.827-104A>G rs111229114 0.03337
NM_000503.6(EYA1):c.418+102C>T rs75142065 0.02732
NM_000503.6(EYA1):c.419-273A>G rs79359169 0.02695
NM_000503.6(EYA1):c.1597+18T>C rs76259565 0.02609
NM_000503.6(EYA1):c.125-31C>T rs113812295 0.01842
NM_000503.6(EYA1):c.1050+28A>C rs7835813 0.01721
NM_000503.6(EYA1):c.1699-3C>T rs117149407 0.01158
NM_000503.6(EYA1):c.840C>A (p.Ile280=) rs55972891 0.00286
NM_000503.6(EYA1):c.1460C>T (p.Ser487Leu) rs139717960 0.00069
NM_000503.6(EYA1):c.782C>T (p.Pro261Leu) rs77825059 0.00069
NM_000503.6(EYA1):c.1050+66T>G rs2305096 0.00058
NM_000503.6(EYA1):c.1699-8T>C rs201537030 0.00048
NM_000503.6(EYA1):c.639+17G>C rs199791692 0.00006
GRCh37/hg19 8q13.3(chr8:72190320-72205191)x1
GRCh37/hg19 8q13.3(chr8:72201726-72213290)x3
GRCh37/hg19 8q13.3(chr8:72201726-72214222)x3
GRCh37/hg19 8q13.3(chr8:72201726-72217690)x3
GRCh37/hg19 8q13.3(chr8:72202074-72217690)x3
GRCh37/hg19 8q13.3(chr8:72202625-72217665)x3
GRCh37/hg19 8q13.3(chr8:72202968-72217690)x3
GRCh37/hg19 8q13.3(chr8:72204125-72217690)x3
GRCh37/hg19 8q13.3(chr8:72211178-72217690)x1
GRCh37/hg19 8q13.3(chr8:72214786-72225252)x0
GRCh37/hg19 8q13.3(chr8:72214786-72225345)x1
GRCh37/hg19 8q13.3(chr8:72259845-72272544)x3
GRCh37/hg19 8q13.3(chr8:72259845-72280705)x3
NM_000503.6(EYA1):c.-340G>T rs55997623
NM_000503.6(EYA1):c.1051-323C>G rs116950892
NM_000503.6(EYA1):c.1360+286_1360+303dup rs61175547
NM_000503.6(EYA1):c.1598-326C>G rs7818376
NM_000503.6(EYA1):c.272+99A>T rs75686418
NM_000503.6(EYA1):c.826+104C>T rs17783968
NM_000503.6(EYA1):c.966+233_966+236del rs199972984

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