ClinVar Miner

List of variants in gene EPHA2 reported as benign by PreventionGenetics, part of Exact Sciences

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_004431.5(EPHA2):c.987C>T (p.Pro329=) rs2230597 0.37785
NM_004431.5(EPHA2):c.573G>A (p.Leu191=) rs6678616 0.27639
NM_004431.5(EPHA2):c.570G>A (p.Ala190=) rs6678618 0.26138
NM_004431.5(EPHA2):c.2874C>T (p.Ile958=) rs3754334 0.23636
NM_004431.5(EPHA2):c.1738+16C>T rs6669624 0.19542
NM_004431.5(EPHA2):c.1983C>T (p.Leu661=) rs10907223 0.15604
NM_004431.5(EPHA2):c.2627G>A (p.Arg876His) rs35903225 0.01759
NM_004431.5(EPHA2):c.824-11G>A rs2291804 0.01705
NM_004431.5(EPHA2):c.1171G>A (p.Gly391Arg) rs34192549 0.01659
NM_004431.5(EPHA2):c.2352C>T (p.Thr784=) rs112285834 0.01597
NM_004431.5(EPHA2):c.648C>T (p.Ala216=) rs34753465 0.00766
NM_004431.5(EPHA2):c.86-9C>T rs138164293 0.00608
NM_004431.5(EPHA2):c.1896G>A (p.Leu632=) rs55655135 0.00541
NM_004431.5(EPHA2):c.493G>A (p.Val165Met) rs150790360 0.00444
NM_004431.5(EPHA2):c.1314G>A (p.Glu438=) rs55700006 0.00355
NM_004431.5(EPHA2):c.1486G>A (p.Asp496Asn) rs115171763 0.00292
NM_004431.5(EPHA2):c.2374C>A (p.Arg792=) rs55869078 0.00255
NM_004431.5(EPHA2):c.489G>A (p.Leu163=) rs146626026 0.00153
NM_004431.5(EPHA2):c.1359C>T (p.Ser453=) rs55740291 0.00039
NM_004431.5(EPHA2):c.1429-4A>G rs374403114 0.00002

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