ClinVar Miner

List of variants in gene IL17F reported as uncertain significance for Candidiasis, familial, 6

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Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_052872.4(IL17F):c.254+1G>T rs117796773 0.00070
NM_052872.4(IL17F):c.53C>T (p.Ser18Leu) rs145598353 0.00046
NM_052872.4(IL17F):c.215G>A (p.Arg72His) rs144854652 0.00031
NM_052872.4(IL17F):c.391C>T (p.Arg131Trp) rs147873628 0.00014
NM_052872.4(IL17F):c.274C>T (p.Arg92Trp) rs142962486 0.00010
NM_052872.4(IL17F):c.243C>G (p.Pro81=) rs769617558 0.00007
NM_052872.4(IL17F):c.284C>T (p.Ser95Leu) rs748486078 0.00006
NM_052872.4(IL17F):c.458C>T (p.Thr153Ile) rs769299818 0.00006
NM_052872.4(IL17F):c.83C>T (p.Ala28Val) rs201102127 0.00006
NM_052872.4(IL17F):c.214C>T (p.Arg72Cys) rs764500129 0.00005
NM_052872.4(IL17F):c.230G>A (p.Arg77His) rs371280410 0.00004
NM_052872.4(IL17F):c.33+5G>A rs374814501 0.00004
NM_052872.4(IL17F):c.275G>A (p.Arg92Gln) rs376780230 0.00003
NM_052872.4(IL17F):c.350C>A (p.Ser117Tyr) rs767452983 0.00003
NM_052872.4(IL17F):c.427T>C (p.Leu143=) rs1015495067 0.00003
NM_052872.4(IL17F):c.104A>G (p.Lys35Arg) rs750915214 0.00002
NM_052872.4(IL17F):c.392G>A (p.Arg131Gln) rs764026426 0.00002
NM_052872.4(IL17F):c.413C>G (p.Ser138Cys) rs1173562555 0.00002
NM_052872.4(IL17F):c.488A>G (p.Gln163Arg) rs571639953 0.00002
NM_052872.4(IL17F):c.121T>A (p.Phe41Ile) rs1764017239 0.00001
NM_052872.4(IL17F):c.140G>T (p.Cys47Phe) rs760922852 0.00001
NM_052872.4(IL17F):c.200G>A (p.Arg67His) rs1235526621 0.00001
NM_052872.4(IL17F):c.308G>A (p.Arg103Lys) rs766577007 0.00001
NM_052872.4(IL17F):c.361G>A (p.Val121Ile) rs550486674 0.00001
NM_052872.4(IL17F):c.3G>C (p.Met1Ile) rs752517532 0.00001
NM_052872.4(IL17F):c.428T>G (p.Leu143Trp) rs774103459 0.00001
NM_052872.4(IL17F):c.469C>T (p.Pro157Ser) rs144576902 0.00001
NM_052872.4(IL17F):c.489G>C (p.Gln163His) rs1169477692 0.00001
NM_052872.4(IL17F):c.91C>T (p.Arg31Trp) rs377717323 0.00001
NC_000006.12:g.(?_52236911)_(52244449_?)dup
NM_052872.4(IL17F):c.-6C>T rs764936954
NM_052872.4(IL17F):c.112C>T (p.His38Tyr)
NM_052872.4(IL17F):c.115A>G (p.Thr39Ala) rs1436156723
NM_052872.4(IL17F):c.116C>T (p.Thr39Ile)
NM_052872.4(IL17F):c.11A>G (p.Lys4Arg)
NM_052872.4(IL17F):c.123C>G (p.Phe41Leu) rs1582260865
NM_052872.4(IL17F):c.125A>T (p.Gln42Leu)
NM_052872.4(IL17F):c.12G>C (p.Lys4Asn) rs2128268858
NM_052872.4(IL17F):c.130C>T (p.Pro44Ser)
NM_052872.4(IL17F):c.133G>A (p.Glu45Lys)
NM_052872.4(IL17F):c.134A>G (p.Glu45Gly)
NM_052872.4(IL17F):c.137G>A (p.Ser46Asn)
NM_052872.4(IL17F):c.142C>T (p.Pro48Ser)
NM_052872.4(IL17F):c.181A>G (p.Ile61Val) rs1488403842
NM_052872.4(IL17F):c.182T>A (p.Ile61Asn)
NM_052872.4(IL17F):c.199C>A (p.Arg67Ser) rs754476266
NM_052872.4(IL17F):c.199C>T (p.Arg67Cys)
NM_052872.4(IL17F):c.202G>A (p.Val68Ile)
NM_052872.4(IL17F):c.208A>G (p.Met70Val) rs764517083
NM_052872.4(IL17F):c.223G>A (p.Glu75Lys) rs373228601
NM_052872.4(IL17F):c.229C>A (p.Arg77Ser)
NM_052872.4(IL17F):c.233C>A (p.Ser78Tyr) rs1764012735
NM_052872.4(IL17F):c.235A>C (p.Thr79Pro)
NM_052872.4(IL17F):c.241C>T (p.Pro81Ser)
NM_052872.4(IL17F):c.254+10A>G rs754360019
NM_052872.4(IL17F):c.254+1G>A rs117796773
NM_052872.4(IL17F):c.254+5G>T
NM_052872.4(IL17F):c.254C>T (p.Thr85Ile)
NM_052872.4(IL17F):c.255-3C>T
NM_052872.4(IL17F):c.273C>G (p.Asn91Lys) rs775184787
NM_052872.4(IL17F):c.298G>T (p.Ala100Ser)
NM_052872.4(IL17F):c.305G>A (p.Cys102Tyr)
NM_052872.4(IL17F):c.31A>G (p.Met11Val)
NM_052872.4(IL17F):c.329C>T (p.Ala110Val)
NM_052872.4(IL17F):c.34-1G>A
NM_052872.4(IL17F):c.345C>A (p.Asp115Glu) rs137981743
NM_052872.4(IL17F):c.347T>G (p.Ile116Ser) rs1042175463
NM_052872.4(IL17F):c.352A>C (p.Met118Leu) rs1763977355
NM_052872.4(IL17F):c.374A>G (p.Gln125Arg) rs1763976446
NM_052872.4(IL17F):c.37A>G (p.Lys13Glu) rs1764019547
NM_052872.4(IL17F):c.380C>A (p.Thr127Asn)
NM_052872.4(IL17F):c.388G>A (p.Val130Ile) rs141798304
NM_052872.4(IL17F):c.388G>T (p.Val130Phe) rs141798304
NM_052872.4(IL17F):c.402C>G (p.His134Gln)
NM_052872.4(IL17F):c.403C>G (p.Gln135Glu) rs969467406
NM_052872.4(IL17F):c.404A>G (p.Gln135Arg)
NM_052872.4(IL17F):c.437T>G (p.Val146Gly) rs1763973005
NM_052872.4(IL17F):c.456C>T (p.Cys152=) rs1345707985
NM_052872.4(IL17F):c.469C>G (p.Pro157Ala) rs144576902
NM_052872.4(IL17F):c.53C>A (p.Ser18Ter) rs145598353
NM_052872.4(IL17F):c.56T>C (p.Ile19Thr) rs1764019189
NM_052872.4(IL17F):c.67G>C (p.Ala23Pro)
NM_052872.4(IL17F):c.68C>T (p.Ala23Val)
NM_052872.4(IL17F):c.84_85delinsTT (p.Ala29Ser) rs2128267832
NM_052872.4(IL17F):c.92G>A (p.Arg31Gln)
NM_052872.4(IL17F):c.97del (p.Ile33fs)
NM_052872.4(IL17F):c.99C>G (p.Ile33Met) rs1764017856

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