ClinVar Miner

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

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Gene type:
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Total variants: 40
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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.2904G>C (p.Gln968His) rs138818894 0.00159
NM_004431.5(EPHA2):c.489G>A (p.Leu163=) rs146626026 0.00153
NM_004431.5(EPHA2):c.2097C>T (p.Ala699=) rs149080726 0.00152
NM_004431.5(EPHA2):c.944G>A (p.Arg315Gln) rs139176878 0.00147
NM_004431.5(EPHA2):c.2100G>A (p.Leu700=) rs141594918 0.00103
NM_004431.5(EPHA2):c.2162G>A (p.Arg721Gln) rs116506614 0.00073
NM_004431.5(EPHA2):c.453C>T (p.Thr151=) rs139200871 0.00060
NM_004431.5(EPHA2):c.1359C>T (p.Ser453=) rs55740291 0.00039
NM_004431.5(EPHA2):c.2875G>A (p.Ala959Thr) rs139787163 0.00036
NM_004431.5(EPHA2):c.2826C>T (p.Asp942=) rs143828420 0.00011
NM_004431.5(EPHA2):c.1567G>A (p.Glu523Lys) rs369180720 0.00008
NM_004431.5(EPHA2):c.1533G>A (p.Thr511=) rs550085875 0.00004
NM_004431.5(EPHA2):c.1429-4A>G rs374403114 0.00002
NM_004431.5(EPHA2):c.154-5C>A
NM_004431.5(EPHA2):c.1582+6T>C
NM_004431.5(EPHA2):c.168G>A (p.Gln56=)
NM_004431.5(EPHA2):c.2455T>G (p.Trp819Gly)
NM_004431.5(EPHA2):c.2463G>A (p.Leu821=) rs143247718
NM_004431.5(EPHA2):c.2719C>T (p.Arg907Cys)
NM_004431.5(EPHA2):c.2725G>A (p.Val909Met)
NM_004431.5(EPHA2):c.2928_2929del (p.Ile976fs)
NM_004431.5(EPHA2):c.411C>G (p.Arg137=)
NM_004431.5(EPHA2):c.921C>T (p.Cys307=)

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