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33 records found for search term Il33
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150445080CV1278093single nucleotide variantNM_033439.4(IL33):c.91+1165C>Tnot provided [RCV001707236]benign962429506242950Humanname
155967047CV2391302single nucleotide variantNM_033439.4(IL33):c.10A>G (p.Lys4Glu)not specified [RCV004237667]uncertain significance962417046241704Humanname
597774919CV3686542single nucleotide variantNM_033439.4(IL33):c.11A>C (p.Lys4Thr)not specified [RCV004929223]uncertain significance962417056241705Humanname
15163058CV711995single nucleotide variantNM_033439.4(IL33):c.150C>A (p.Gly50=)not provided [RCV000970400]benign962505326250532Humanname
15151570CV737161single nucleotide variantNM_033439.4(IL33):c.273G>C (p.Val91=)not provided [RCV000901390]benign962511956251195Humanname
156391249CV2385196single nucleotide variantNM_033439.4(IL33):c.43G>A (p.Ala15Thr)not specified [RCV004228445]uncertain significance962417376241737Humanname
405804975CV3271207single nucleotide variantNM_033439.4(IL33):c.47A>G (p.Lys16Arg)not specified [RCV004405268]uncertain significance962417416241741Humanname
598207619CV3972294single nucleotide variantNM_033439.4(IL33):c.84G>C (p.Lys28Asn)not specified [RCV005338002]uncertain significance962417786241778Humanname
156210301CV2314233single nucleotide variantNM_033439.4(IL33):c.296C>T (p.Ser99Leu)not specified [RCV004166602]uncertain significance962512186251218Humanname
155916806CV2336210single nucleotide variantNM_033439.4(IL33):c.164A>G (p.Lys55Arg)not specified [RCV004191967]uncertain significance962505466250546Humanname
329356476CV2430769single nucleotide variantNM_033439.4(IL33):c.142C>T (p.Arg48Cys)not specified [RCV004253947]uncertain significance962505246250524Humanname
401767782CV2677814single nucleotide variantNM_033439.4(IL33):c.244C>T (p.Leu82Phe)not specified [RCV004294312]likely benign962511666251166Humanname
405804969CV3271204single nucleotide variantNM_033439.4(IL33):c.266C>T (p.Ser89Phe)not specified [RCV004405265]uncertain significance962511886251188Humanname
9687106CV171469single nucleotide variantNM_033439.4(IL33):c.712G>A (p.Val238Met)Prostate cancer [RCV000149325]uncertain significance962560676256067Human2name
155968760CV2262030single nucleotide variantNM_033439.4(IL33):c.571G>C (p.Asp191His)not specified [RCV004126513]uncertain significance962545126254512Humanname
329396928CV2463666single nucleotide variantNM_033439.4(IL33):c.757G>C (p.Asp253His)not specified [RCV004277459]uncertain significance962561126256112Humanname
401761885CV2713933single nucleotide variantNM_033439.4(IL33):c.610G>A (p.Glu204Lys)not specified [RCV004315358]uncertain significance962545516254551Humanname
405804971CV3271205single nucleotide variantNM_033439.4(IL33):c.471T>G (p.Asp157Glu)not specified [RCV004405266]uncertain significance962535536253553Humanname
405804973CV3271206single nucleotide variantNM_033439.4(IL33):c.478T>A (p.Leu160Ile)not specified [RCV004405267]uncertain significance962535606253560Humanname
405804977CV3271208single nucleotide variantNM_033439.4(IL33):c.536G>C (p.Gly179Ala)not specified [RCV004405269]uncertain significance962544776254477Humanname
407516028CV3444616single nucleotide variantNM_033439.4(IL33):c.719T>C (p.Ile240Thr)not specified [RCV004628061]uncertain significance962560746256074Humanname
407516031CV3444617single nucleotide variantNM_033439.4(IL33):c.299G>A (p.Gly100Glu)not specified [RCV004628062]uncertain significance962512216251221Humanname
597774899CV3686537single nucleotide variantNM_033439.4(IL33):c.471T>A (p.Asp157Glu)not specified [RCV004929218]uncertain significance962535536253553Humanname
597774903CV3686538single nucleotide variantNM_033439.4(IL33):c.457G>C (p.Asp153His)not specified [RCV004929219]uncertain significance962529796252979Humanname
597774907CV3686539single nucleotide variantNM_033439.4(IL33):c.331T>A (p.Ser111Thr)not specified [RCV004929220]uncertain significance962512536251253Humanname
597774911CV3686540single nucleotide variantNM_033439.4(IL33):c.689T>C (p.Phe230Ser)not specified [RCV004929221]uncertain significance962560446256044Humanname
597774915CV3686541single nucleotide variantNM_033439.4(IL33):c.409G>A (p.Ala137Thr)not specified [RCV004929222]uncertain significance962529316252931Humanname
598207627CV3972295single nucleotide variantNM_033439.4(IL33):c.437A>G (p.Tyr146Cys)not specified [RCV005338003]uncertain significance962529596252959Humanname
598180203CV3972296single nucleotide variantNM_033439.4(IL33):c.560G>A (p.Ser187Asn)not specified [RCV005352301]uncertain significance962545016254501Humanname
598180210CV3972297single nucleotide variantNM_033439.4(IL33):c.355A>G (p.Ile119Val)not specified [RCV005352302]likely benign962528776252877Humanname
15198260CV701027single nucleotide variantNM_033439.4(IL33):c.789C>G (p.Ile263Met)not provided [RCV000956701]benign962561446256144Humanname
15134266CV711996single nucleotide variantNM_033439.4(IL33):c.457G>T (p.Asp153Tyr)not provided [RCV000965097]benign962529796252979Humanname
15184820CV711997single nucleotide variantNM_033439.4(IL33):c.603C>G (p.His201Gln)not provided [RCV000975205]benign962545446254544Humanname