ClinVar Miner

List of variants in gene EPHA3 reported by Ambry Genetics

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Gene type:
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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_005233.6(EPHA3):c.1325C>T (p.Thr442Met) rs112239794 0.00034
NM_005233.6(EPHA3):c.1130G>A (p.Ser377Asn) rs200415022 0.00015
NM_005233.6(EPHA3):c.919G>A (p.Glu307Lys) rs148593404 0.00006
NM_005233.6(EPHA3):c.1574A>T (p.Glu525Val) rs150469112 0.00005
NM_005233.6(EPHA3):c.2051G>A (p.Arg684Gln) rs372257039 0.00005
NM_005233.6(EPHA3):c.1775G>A (p.Gly592Asp) rs534679111 0.00003
NM_005233.6(EPHA3):c.2656G>T (p.Gly886Cys) rs373736475 0.00003
NM_005233.6(EPHA3):c.2872G>A (p.Val958Met) rs762601076 0.00003
NM_005233.6(EPHA3):c.338T>C (p.Leu113Ser) rs537025827 0.00003
NM_005233.6(EPHA3):c.49G>C (p.Asp17His) rs201110271 0.00002
NM_005233.6(EPHA3):c.1090A>C (p.Lys364Gln) rs773454441 0.00001
NM_005233.6(EPHA3):c.1280C>T (p.Ala427Val) rs530556931 0.00001
NM_005233.6(EPHA3):c.1411G>C (p.Glu471Gln) rs537923825 0.00001
NM_005233.6(EPHA3):c.1648G>C (p.Ala550Pro) rs371462790 0.00001
NM_005233.6(EPHA3):c.1691T>C (p.Ile564Thr) rs536008328 0.00001
NM_005233.6(EPHA3):c.1757G>A (p.Gly586Glu) rs778106353 0.00001
NM_005233.6(EPHA3):c.1768C>T (p.Leu590Phe) rs567496673 0.00001
NM_005233.6(EPHA3):c.2003T>C (p.Leu668Pro) rs748606864 0.00001
NM_005233.6(EPHA3):c.2087T>C (p.Met696Thr) rs1225397244 0.00001
NM_005233.6(EPHA3):c.2134C>T (p.Arg712Cys) rs777211567 0.00001
NM_005233.6(EPHA3):c.2924A>G (p.Gln975Arg) rs755942381 0.00001
NM_005233.6(EPHA3):c.631A>G (p.Met211Val) rs1413376820 0.00001
NM_005233.6(EPHA3):c.698A>G (p.Asn233Ser) rs758441001 0.00001
NM_005233.6(EPHA3):c.1025T>C (p.Ile342Thr)
NM_005233.6(EPHA3):c.135C>G (p.Ile45Met) rs139262347
NM_005233.6(EPHA3):c.1426G>A (p.Glu476Lys)
NM_005233.6(EPHA3):c.1505A>G (p.Asp502Gly)
NM_005233.6(EPHA3):c.1553G>A (p.Gly518Glu)
NM_005233.6(EPHA3):c.1562G>A (p.Ser521Asn)
NM_005233.6(EPHA3):c.1636G>A (p.Ala546Thr)
NM_005233.6(EPHA3):c.1669A>C (p.Thr557Pro)
NM_005233.6(EPHA3):c.1801A>G (p.Thr601Ala)
NM_005233.6(EPHA3):c.1954A>C (p.Ile652Leu) rs779822883
NM_005233.6(EPHA3):c.2083G>C (p.Val695Leu)
NM_005233.6(EPHA3):c.2221G>T (p.Gly741Cys)
NM_005233.6(EPHA3):c.2275G>A (p.Val759Met) rs146856660
NM_005233.6(EPHA3):c.2303C>T (p.Ser768Leu)
NM_005233.6(EPHA3):c.2399A>T (p.Lys800Met)
NM_005233.6(EPHA3):c.2536C>G (p.Pro846Ala) rs142030914
NM_005233.6(EPHA3):c.2560T>C (p.Tyr854His)
NM_005233.6(EPHA3):c.2644A>T (p.Ile882Phe)
NM_005233.6(EPHA3):c.266G>A (p.Arg89Lys)
NM_005233.6(EPHA3):c.2684C>T (p.Ala895Val) rs141716319
NM_005233.6(EPHA3):c.2780A>G (p.His927Arg) rs2472121799
NM_005233.6(EPHA3):c.568G>A (p.Val190Ile) rs2107182688
NM_005233.6(EPHA3):c.61G>A (p.Glu21Lys)
NM_005233.6(EPHA3):c.800G>A (p.Gly267Asp)
NM_005233.6(EPHA3):c.802T>C (p.Phe268Leu)
NM_005233.6(EPHA3):c.899G>C (p.Gly300Ala)
NM_005233.6(EPHA3):c.955T>C (p.Ser319Pro)

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