ClinVar Miner

List of variants in gene EGLN1 reported as uncertain significance by Invitae

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Gene type:
ClinVar version:
Total variants: 158
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HGVS dbSNP gnomAD frequency
NM_022051.3(EGLN1):c.287C>T (p.Ala96Val) rs113401862 0.00236
NM_022051.3(EGLN1):c.311C>T (p.Ser104Phe) rs551207815 0.00113
NM_022051.3(EGLN1):c.359C>T (p.Pro120Leu) rs796280222 0.00026
NM_022051.3(EGLN1):c.558G>C (p.Lys186Asn) rs201365992 0.00018
NM_022051.3(EGLN1):c.276G>C (p.Glu92Asp) rs992728216 0.00014
NM_022051.3(EGLN1):c.41G>A (p.Ser14Asn) rs761497751 0.00014
NM_022051.3(EGLN1):c.419C>T (p.Ala140Val) rs768557500 0.00009
NM_022051.3(EGLN1):c.735T>G (p.Ser245Arg) rs764531356 0.00008
NM_022051.3(EGLN1):c.205G>C (p.Val69Leu) rs931430574 0.00006
NM_022051.3(EGLN1):c.457T>C (p.Ser153Pro) rs963834004 0.00006
NM_022051.3(EGLN1):c.8A>G (p.Asn3Ser) rs879573663 0.00006
NM_022051.3(EGLN1):c.325A>G (p.Lys109Glu) rs891489163 0.00005
NM_022051.3(EGLN1):c.575A>G (p.Lys192Arg) rs75538505 0.00005
NM_022051.3(EGLN1):c.1244A>G (p.Asn415Ser) rs748926816 0.00004
NM_022051.3(EGLN1):c.763A>G (p.Lys255Glu) rs767916069 0.00003
NM_022051.3(EGLN1):c.1216+6C>T rs376628693 0.00002
NM_022051.3(EGLN1):c.1273G>A (p.Val425Ile) rs1472408827 0.00002
NM_022051.3(EGLN1):c.319G>T (p.Ala107Ser) rs531081279 0.00002
NM_022051.3(EGLN1):c.350C>T (p.Pro117Leu) rs1050394369 0.00002
NM_022051.3(EGLN1):c.386C>T (p.Ala129Val) rs1380554913 0.00002
NM_022051.3(EGLN1):c.405C>T (p.Gly135=) rs781566823 0.00002
NM_022051.3(EGLN1):c.515C>T (p.Ala172Val) rs777466821 0.00002
NM_022051.3(EGLN1):c.917A>G (p.Asn306Ser) rs560996946 0.00002
NM_022051.3(EGLN1):c.934C>T (p.Arg312Cys) rs748814440 0.00002
NM_022051.3(EGLN1):c.103C>G (p.Arg35Gly) rs778100040 0.00001
NM_022051.3(EGLN1):c.1234G>A (p.Val412Ile) rs768347513 0.00001
NM_022051.3(EGLN1):c.1264G>A (p.Gly422Ser) rs753505082 0.00001
NM_022051.3(EGLN1):c.190G>A (p.Ala64Thr) rs776333127 0.00001
NM_022051.3(EGLN1):c.202G>C (p.Gly68Arg) rs763530007 0.00001
NM_022051.3(EGLN1):c.245C>T (p.Ala82Val) rs771498926 0.00001
NM_022051.3(EGLN1):c.261G>C (p.Arg87Ser) rs1024909187 0.00001
NM_022051.3(EGLN1):c.272G>A (p.Arg91Gln) rs1180795317 0.00001
NM_022051.3(EGLN1):c.32C>T (p.Pro11Leu) rs1198122970 0.00001
NM_022051.3(EGLN1):c.345G>T (p.Lys115Asn) rs1307321781 0.00001
NM_022051.3(EGLN1):c.371C>T (p.Ala124Val) rs972861708 0.00001
NM_022051.3(EGLN1):c.445C>A (p.Pro149Thr) rs374893731 0.00001
NM_022051.3(EGLN1):c.491C>T (p.Pro164Leu) rs770213782 0.00001
NM_022051.3(EGLN1):c.634G>A (p.Asp212Asn) rs376247953 0.00001
NM_022051.3(EGLN1):c.925G>T (p.Gly309Cys) rs774056264 0.00001
NM_022051.3(EGLN1):c.95G>A (p.Arg32His) rs867477927 0.00001
NC_000001.10:g.(?_231502157)_(231557634_?)dup
NM_022051.3(EGLN1):c.*68G>A
NM_022051.3(EGLN1):c.*92G>C
NM_022051.3(EGLN1):c.1012G>C (p.Val338Leu) rs1687797398
NM_022051.3(EGLN1):c.1018G>A (p.Gly340Arg) rs2102894569
NM_022051.3(EGLN1):c.1022G>C (p.Gly341Ala)
NM_022051.3(EGLN1):c.1026A>G (p.Ile342Met) rs1156457644
NM_022051.3(EGLN1):c.103C>T (p.Arg35Cys)
NM_022051.3(EGLN1):c.104G>A (p.Arg35His)
NM_022051.3(EGLN1):c.104G>T (p.Arg35Leu)
NM_022051.3(EGLN1):c.1108C>T (p.Arg370Cys)
NM_022051.3(EGLN1):c.1132C>T (p.Pro378Ser)
NM_022051.3(EGLN1):c.116C>T (p.Ser39Phe)
NM_022051.3(EGLN1):c.1182T>A (p.Asp394Glu) rs1572014723
NM_022051.3(EGLN1):c.1193G>A (p.Arg398Gln)
NM_022051.3(EGLN1):c.1201G>A (p.Val401Ile) rs771491532
NM_022051.3(EGLN1):c.1208A>G (p.Tyr403Cys)
NM_022051.3(EGLN1):c.122_124del (p.Tyr41del) rs1182227189
NM_022051.3(EGLN1):c.1234dup (p.Val412fs)
NM_022051.3(EGLN1):c.1250C>T (p.Pro417Leu) rs1293477221
NM_022051.3(EGLN1):c.1265G>T (p.Gly422Val)
NM_022051.3(EGLN1):c.1279T>C (p.Ter427Gln) rs767020788
NM_022051.3(EGLN1):c.131A>G (p.Lys44Arg)
NM_022051.3(EGLN1):c.135G>T (p.Glu45Asp) rs2102948215
NM_022051.3(EGLN1):c.140A>G (p.Gln47Arg) rs73121547
NM_022051.3(EGLN1):c.154A>G (p.Lys52Glu)
NM_022051.3(EGLN1):c.15CGGCGGGCC[1] (p.6GGP[1])
NM_022051.3(EGLN1):c.15CGGCGGGCC[3] (p.Pro11_Ser12insGlyGlyPro)
NM_022051.3(EGLN1):c.164A>G (p.Lys55Arg)
NM_022051.3(EGLN1):c.179G>T (p.Gly60Val)
NM_022051.3(EGLN1):c.186G>C (p.Glu62Asp)
NM_022051.3(EGLN1):c.187G>A (p.Gly63Ser)
NM_022051.3(EGLN1):c.199C>T (p.His67Tyr)
NM_022051.3(EGLN1):c.202G>A (p.Gly68Arg)
NM_022051.3(EGLN1):c.204A>T (p.Gly68=) rs760247413
NM_022051.3(EGLN1):c.209G>A (p.Gly70Asp)
NM_022051.3(EGLN1):c.224C>G (p.Ser75Cys)
NM_022051.3(EGLN1):c.226G>A (p.Gly76Ser) rs1224937631
NM_022051.3(EGLN1):c.227G>T (p.Gly76Val)
NM_022051.3(EGLN1):c.229C>T (p.Pro77Ser) rs920027770
NM_022051.3(EGLN1):c.230C>T (p.Pro77Leu)
NM_022051.3(EGLN1):c.232G>A (p.Ala78Thr) rs1656619749
NM_022051.3(EGLN1):c.242C>G (p.Ala81Gly)
NM_022051.3(EGLN1):c.243_257dup (p.Pro86_Arg87insAlaValProProPro)
NM_022051.3(EGLN1):c.247G>A (p.Val83Met) rs1451855470
NM_022051.3(EGLN1):c.256C>G (p.Pro86Ala) rs1487874168
NM_022051.3(EGLN1):c.259A>G (p.Arg87Gly) rs1167403455
NM_022051.3(EGLN1):c.263C>G (p.Ala88Gly)
NM_022051.3(EGLN1):c.271C>T (p.Arg91Trp)
NM_022051.3(EGLN1):c.275A>C (p.Glu92Ala)
NM_022051.3(EGLN1):c.277C>T (p.Pro93Ser)
NM_022051.3(EGLN1):c.295C>T (p.Arg99Cys) rs2102947932
NM_022051.3(EGLN1):c.305A>G (p.Asn102Ser)
NM_022051.3(EGLN1):c.313G>A (p.Gly105Arg)
NM_022051.3(EGLN1):c.329G>T (p.Gly110Val)
NM_022051.3(EGLN1):c.340G>A (p.Ala114Thr)
NM_022051.3(EGLN1):c.345G>C (p.Lys115Asn) rs1307321781
NM_022051.3(EGLN1):c.346C>A (p.Pro116Thr) rs944307657
NM_022051.3(EGLN1):c.347C>T (p.Pro116Leu)
NM_022051.3(EGLN1):c.349C>T (p.Pro117Ser)
NM_022051.3(EGLN1):c.352G>T (p.Ala118Ser) rs1656606563
NM_022051.3(EGLN1):c.353C>A (p.Ala118Asp) rs1357444347
NM_022051.3(EGLN1):c.362C>G (p.Ala121Gly) rs1312410428
NM_022051.3(EGLN1):c.366_389del (p.Ala124_Ala131del)
NM_022051.3(EGLN1):c.366_389dup (p.Ala124_Ala131dup) rs1470968362
NM_022051.3(EGLN1):c.37C>G (p.Pro13Ala)
NM_022051.3(EGLN1):c.382C>A (p.Arg128Ser) rs756094298
NM_022051.3(EGLN1):c.382C>G (p.Arg128Gly)
NM_022051.3(EGLN1):c.382C>T (p.Arg128Cys)
NM_022051.3(EGLN1):c.3G>T (p.Met1Ile) rs1308120626
NM_022051.3(EGLN1):c.404G>A (p.Gly135Asp) rs1176313181
NM_022051.3(EGLN1):c.413T>C (p.Val138Ala) rs1408448213
NM_022051.3(EGLN1):c.413T>G (p.Val138Gly)
NM_022051.3(EGLN1):c.415G>A (p.Ala139Thr)
NM_022051.3(EGLN1):c.416C>T (p.Ala139Val)
NM_022051.3(EGLN1):c.424G>A (p.Ala142Thr)
NM_022051.3(EGLN1):c.425C>G (p.Ala142Gly)
NM_022051.3(EGLN1):c.428A>T (p.Glu143Val)
NM_022051.3(EGLN1):c.430C>G (p.Pro144Ala)
NM_022051.3(EGLN1):c.433G>C (p.Gly145Arg)
NM_022051.3(EGLN1):c.436A>C (p.Lys146Gln)
NM_022051.3(EGLN1):c.440A>G (p.Glu147Gly)
NM_022051.3(EGLN1):c.449C>T (p.Pro150Leu) rs758337994
NM_022051.3(EGLN1):c.454C>A (p.Arg152Ser) rs1200860908
NM_022051.3(EGLN1):c.454C>G (p.Arg152Gly)
NM_022051.3(EGLN1):c.454C>T (p.Arg152Cys)
NM_022051.3(EGLN1):c.458C>T (p.Ser153Leu)
NM_022051.3(EGLN1):c.472_474del (p.Glu158del)
NM_022051.3(EGLN1):c.477G>T (p.Lys159Asn) rs766985056
NM_022051.3(EGLN1):c.487T>G (p.Tyr163Asp)
NM_022051.3(EGLN1):c.490C>A (p.Pro164Thr) rs1407678909
NM_022051.3(EGLN1):c.490C>T (p.Pro164Ser)
NM_022051.3(EGLN1):c.493C>A (p.Pro165Thr)
NM_022051.3(EGLN1):c.493C>G (p.Pro165Ala) rs200502960
NM_022051.3(EGLN1):c.496A>G (p.Ser166Gly)
NM_022051.3(EGLN1):c.503C>T (p.Thr168Met)
NM_022051.3(EGLN1):c.508G>C (p.Gly170Arg)
NM_022051.3(EGLN1):c.520A>T (p.Ser174Cys)
NM_022051.3(EGLN1):c.530G>A (p.Gly177Asp)
NM_022051.3(EGLN1):c.538C>T (p.Arg180Trp)
NM_022051.3(EGLN1):c.53G>A (p.Arg18Gln) rs886046112
NM_022051.3(EGLN1):c.541C>T (p.Pro181Ser)
NM_022051.3(EGLN1):c.546C>G (p.Asn182Lys) rs1258825907
NM_022051.3(EGLN1):c.566C>T (p.Pro189Leu)
NM_022051.3(EGLN1):c.568_569delinsTT (p.Ala190Leu) rs1558086261
NM_022051.3(EGLN1):c.569C>G (p.Ala190Gly) rs769931960
NM_022051.3(EGLN1):c.595G>T (p.Val199Leu) rs2102947196
NM_022051.3(EGLN1):c.599C>G (p.Pro200Arg)
NM_022051.3(EGLN1):c.668_673dup (p.Asp224_Glu225insGlyAsp)
NM_022051.3(EGLN1):c.683C>G (p.Ala228Gly)
NM_022051.3(EGLN1):c.706A>G (p.Thr236Ala)
NM_022051.3(EGLN1):c.734G>A (p.Ser245Asn)
NM_022051.3(EGLN1):c.738C>G (p.Asp246Glu)
NM_022051.3(EGLN1):c.740C>G (p.Ser247Trp)
NM_022051.3(EGLN1):c.923C>T (p.Thr308Met)
NM_022051.3(EGLN1):c.973A>C (p.Thr325Pro)
NM_022051.3(EGLN1):c.980T>C (p.Ile327Thr) rs2102898186
NM_022051.3(EGLN1):c.9T>G (p.Asn3Lys)

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