ClinVar Miner

List of variants in gene combination FOXE3, LINC01389 reported by GeneDx

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_012186.3(FOXE3):c.*77A>G rs2820969 0.99594
NM_012186.3(FOXE3):c.*72T>C rs6666370 0.83961
NM_012186.3(FOXE3):c.510C>T (p.Ala170=) rs34082359 0.30320
NM_012186.3(FOXE3):c.-14G>A rs181190356 0.03946
NM_012186.3(FOXE3):c.146G>C (p.Gly49Ala) rs566961335 0.01320
NC_000001.11:g.47416272C>T rs188265445 0.01170
NM_012186.3(FOXE3):c.423G>A (p.Lys141=) rs145081583 0.01025
NM_012186.3(FOXE3):c.16G>A (p.Asp6Asn) rs765169217 0.00805
NM_012186.3(FOXE3):c.618C>G (p.Ala206=) rs189628587 0.00737
NM_012186.3(FOXE3):c.587G>C (p.Gly196Ala) rs281865461 0.00458
NM_012186.3(FOXE3):c.898A>G (p.Ser300Gly) rs552420470 0.00350
NM_012186.3(FOXE3):c.601G>A (p.Val201Met) rs530072475 0.00329
NM_012186.3(FOXE3):c.276C>T (p.Leu92=) rs143712915 0.00124
NM_012186.3(FOXE3):c.158C>T (p.Pro53Leu) rs534479543 0.00083
NM_012186.3(FOXE3):c.234G>A (p.Ala78=) rs201158701 0.00027
NM_012186.3(FOXE3):c.232G>A (p.Ala78Thr) rs377669670 0.00005
NM_012186.3(FOXE3):c.471C>G (p.Asn157Lys) rs749859478 0.00004
NM_012186.3(FOXE3):c.206G>A (p.Arg69His) rs767855430 0.00002
NM_012186.3(FOXE3):c.431A>G (p.Tyr144Cys) rs747148416 0.00001
NM_012186.3(FOXE3):c.617C>A (p.Ala206Asp) rs1011363716 0.00001
NM_012186.3(FOXE3):c.720C>A (p.Cys240Ter) rs80358194 0.00001
NM_012186.3(FOXE3):c.925C>A (p.Pro309Thr) rs1085307504 0.00001
NC_000001.11:g.47416226G>T rs115705313
NC_000001.11:g.47416244dup rs137862650
NC_000001.11:g.47416245C>G rs551340839
NM_012186.3(FOXE3):c.163C>A (p.Pro55Thr) rs1646883185
NM_012186.3(FOXE3):c.179GGC[8] (p.Arg65_Pro66insArgArg) rs775343166
NM_012186.3(FOXE3):c.224C>T (p.Ser75Leu) rs750769299
NM_012186.3(FOXE3):c.238A>T (p.Ile80Phe)
NM_012186.3(FOXE3):c.283G>C (p.Ala95Pro)
NM_012186.3(FOXE3):c.283G>T (p.Ala95Ser) rs2124042280
NM_012186.3(FOXE3):c.473G>A (p.Gly158Asp) rs2124042965
NM_012186.3(FOXE3):c.809T>A (p.Val270Glu) rs2124044494
NM_012186.3(FOXE3):c.932_944del (p.Phe311fs) rs2124045053

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