ClinVar Miner

List of variants in gene combination IFNAR2-IL10RB, IL10RB reported as uncertain significance for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 111
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HGVS dbSNP gnomAD frequency
NM_000628.5(IL10RB):c.*816T>C rs118117891 0.00298
NM_000628.5(IL10RB):c.442G>A (p.Val148Met) rs45545138 0.00125
NM_000628.5(IL10RB):c.174-14T>G rs200472684 0.00046
NM_000628.5(IL10RB):c.718G>A (p.Gly240Ser) rs777514296 0.00025
NM_000628.5(IL10RB):c.215C>T (p.Thr72Met) rs148466782 0.00019
NM_000628.5(IL10RB):c.645C>T (p.Asp215=) rs148468217 0.00019
NM_000628.5(IL10RB):c.763G>A (p.Ala255Thr) rs182875134 0.00016
NM_000628.5(IL10RB):c.953C>T (p.Pro318Leu) rs141414815 0.00014
NM_000628.5(IL10RB):c.954G>A (p.Pro318=) rs374161818 0.00014
NM_000628.5(IL10RB):c.548C>G (p.Pro183Arg) rs141328537 0.00009
NM_000628.5(IL10RB):c.*536G>T rs750248101 0.00008
NM_000628.5(IL10RB):c.804+8G>A rs112943706 0.00007
NM_000628.5(IL10RB):c.946G>A (p.Gly316Arg) rs370841672 0.00007
NM_000628.5(IL10RB):c.*616A>G rs886057009 0.00006
NM_000628.5(IL10RB):c.*761C>T rs567397652 0.00006
NM_000628.5(IL10RB):c.484G>A (p.Gly162Ser) rs770980693 0.00006
NM_000628.5(IL10RB):c.575G>A (p.Arg192Gln) rs147402422 0.00006
NM_000628.5(IL10RB):c.646G>A (p.Glu216Lys) rs45469692 0.00006
NM_000628.5(IL10RB):c.742G>A (p.Val248Ile) rs777216483 0.00006
NM_000628.5(IL10RB):c.*515C>T rs767017864 0.00004
NM_000628.5(IL10RB):c.*365C>T rs886057005 0.00003
NM_000628.5(IL10RB):c.*546G>A rs886057006 0.00003
NM_000628.5(IL10RB):c.795C>A (p.His265Gln) rs373204116 0.00003
NM_000628.5(IL10RB):c.911G>A (p.Ser304Asn) rs762692366 0.00003
NM_000628.5(IL10RB):c.328G>A (p.Asp110Asn) rs757581728 0.00002
NM_000628.5(IL10RB):c.389G>A (p.Arg130His) rs775140370 0.00002
NM_000628.5(IL10RB):c.593G>A (p.Arg198Gln) rs774890824 0.00002
NM_000628.5(IL10RB):c.*519A>G rs1339192870 0.00001
NM_000628.5(IL10RB):c.122A>G (p.Glu41Gly) rs753650110 0.00001
NM_000628.5(IL10RB):c.311C>T (p.Thr104Ile) rs1989178743 0.00001
NM_000628.5(IL10RB):c.421G>A (p.Glu141Lys) rs387907326 0.00001
NM_000628.5(IL10RB):c.446A>G (p.Tyr149Cys) rs1186719026 0.00001
NM_000628.5(IL10RB):c.610T>C (p.Trp204Arg) rs1989311645 0.00001
NM_000628.5(IL10RB):c.641A>G (p.His214Arg) rs949664612 0.00001
NM_000628.5(IL10RB):c.647-14A>C rs45526732 0.00001
NM_000628.5(IL10RB):c.650C>T (p.Thr217Met) rs746250523 0.00001
NM_000628.5(IL10RB):c.673G>A (p.Val225Ile) rs765506701 0.00001
NM_000628.5(IL10RB):c.707T>C (p.Leu236Pro) rs752218442 0.00001
NM_000628.5(IL10RB):c.804G>A (p.Glu268=) rs767451280 0.00001
NM_000628.5(IL10RB):c.889G>A (p.Val297Ile) rs911014085 0.00001
NM_000628.5(IL10RB):c.913G>A (p.Gly305Ser) rs376143910 0.00001
NM_000628.5(IL10RB):c.*17A>G rs886057003
NM_000628.5(IL10RB):c.*20C>T rs886057004
NM_000628.5(IL10RB):c.*593TC[1] rs886057007
NM_000628.5(IL10RB):c.*616del rs5843596
NM_000628.5(IL10RB):c.*796T>C rs886057010
NM_000628.5(IL10RB):c.107A>C (p.Asn36Thr) rs2123561113
NM_000628.5(IL10RB):c.116A>G (p.Gln39Arg)
NM_000628.5(IL10RB):c.157A>C (p.Thr53Pro) rs1989015732
NM_000628.5(IL10RB):c.179G>C (p.Arg60Thr)
NM_000628.5(IL10RB):c.194A>G (p.Lys65Arg) rs1269352420
NM_000628.5(IL10RB):c.203A>T (p.Asn68Ile)
NM_000628.5(IL10RB):c.274G>C (p.Glu92Gln) rs2123573879
NM_000628.5(IL10RB):c.284A>T (p.Asp95Val)
NM_000628.5(IL10RB):c.298T>G (p.Trp100Gly) rs868604197
NM_000628.5(IL10RB):c.301G>C (p.Val101Leu)
NM_000628.5(IL10RB):c.302T>C (p.Val101Ala) rs2123573917
NM_000628.5(IL10RB):c.331+4A>T
NM_000628.5(IL10RB):c.332-11C>T rs531765635
NM_000628.5(IL10RB):c.332C>G (p.Thr111Ser) rs769595310
NM_000628.5(IL10RB):c.343C>A (p.Pro115Thr)
NM_000628.5(IL10RB):c.367C>T (p.Leu123Phe) rs1989246173
NM_000628.5(IL10RB):c.377C>T (p.Ser126Phe)
NM_000628.5(IL10RB):c.383A>T (p.His128Leu)
NM_000628.5(IL10RB):c.386T>G (p.Met129Arg) rs759321517
NM_000628.5(IL10RB):c.435G>A (p.Met145Ile)
NM_000628.5(IL10RB):c.466G>A (p.Val156Met)
NM_000628.5(IL10RB):c.498G>A (p.Lys166=)
NM_000628.5(IL10RB):c.498G>C (p.Lys166Asn) rs1989249790
NM_000628.5(IL10RB):c.511C>A (p.Pro171Thr) rs752902509
NM_000628.5(IL10RB):c.511C>T (p.Pro171Ser)
NM_000628.5(IL10RB):c.537A>C (p.Arg179Ser) rs1989309241
NM_000628.5(IL10RB):c.568C>G (p.Gln190Glu)
NM_000628.5(IL10RB):c.584T>C (p.Leu195Pro)
NM_000628.5(IL10RB):c.598A>G (p.Lys200Glu)
NM_000628.5(IL10RB):c.60G>A (p.Met20Ile)
NM_000628.5(IL10RB):c.612G>T (p.Trp204Cys)
NM_000628.5(IL10RB):c.641A>C (p.His214Pro) rs949664612
NM_000628.5(IL10RB):c.647-3C>T rs1989409135
NM_000628.5(IL10RB):c.651G>A (p.Thr217=)
NM_000628.5(IL10RB):c.652G>A (p.Val218Ile) rs776085475
NM_000628.5(IL10RB):c.680T>A (p.Leu227His)
NM_000628.5(IL10RB):c.682A>T (p.Met228Leu) rs376920653
NM_000628.5(IL10RB):c.691G>A (p.Val231Ile)
NM_000628.5(IL10RB):c.715C>A (p.Leu239Ile) rs1601835501
NM_000628.5(IL10RB):c.727G>A (p.Ala243Thr) rs1058861
NM_000628.5(IL10RB):c.738G>T (p.Trp246Cys) rs368740217
NM_000628.5(IL10RB):c.785T>G (p.Leu262Arg) rs1989413733
NM_000628.5(IL10RB):c.787C>G (p.Pro263Ala)
NM_000628.5(IL10RB):c.791A>G (p.Gln264Arg)
NM_000628.5(IL10RB):c.79G>C (p.Val27Leu) rs1989013782
NM_000628.5(IL10RB):c.800_801del (p.Lys267fs) rs1989414348
NM_000628.5(IL10RB):c.823C>T (p.His275Tyr)
NM_000628.5(IL10RB):c.830C>T (p.Thr277Ile) rs756566292
NM_000628.5(IL10RB):c.832del (p.Leu278fs) rs1601839547
NM_000628.5(IL10RB):c.833T>C (p.Leu278Pro)
NM_000628.5(IL10RB):c.833T>G (p.Leu278Arg) rs781553501
NM_000628.5(IL10RB):c.839T>C (p.Phe280Ser) rs2082965278
NM_000628.5(IL10RB):c.841T>G (p.Phe281Val) rs2082965287
NM_000628.5(IL10RB):c.857C>T (p.Ser286Leu) rs771890796
NM_000628.5(IL10RB):c.85A>G (p.Met29Val) rs975065416
NM_000628.5(IL10RB):c.862G>A (p.Glu288Lys) rs2082965441
NM_000628.5(IL10RB):c.863A>T (p.Glu288Val)
NM_000628.5(IL10RB):c.871G>A (p.Val291Ile) rs2082965493
NM_000628.5(IL10RB):c.917A>G (p.Lys306Arg) rs2082965718
NM_000628.5(IL10RB):c.91T>A (p.Ser31Thr) rs1989013997
NM_000628.5(IL10RB):c.933C>A (p.Asp311Glu) rs2082965805
NM_000628.5(IL10RB):c.949A>T (p.Thr317Ser) rs1601839637
NM_000628.5(IL10RB):c.962_967del (p.Gln321_Gly322del) rs2082965983
NM_000628.5(IL10RB):c.970C>T (p.Gln324Ter) rs2082966126
NM_000628.5(IL10RB):c.971A>G (p.Gln324Arg)

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