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30 records found for search term Il1a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405272955CV3220441single nucleotide variantNM_000575.5(IL1A):c.*10C>TIL1A-related disorder [RCV003972265]likely benign2112775057112775057Humanname , trait , alternate_id
150431219CV1235375duplicationNM_000575.5(IL1A):c.*925_*928dupnot provided [RCV001641745]benign2112774138112774139Humanname
15195582CV696978single nucleotide variantNM_000575.5(IL1A):c.276C>T (p.Ile92=)not provided [RCV000955961]benign2112781647112781647Humanname
401869037CV2766847single nucleotide variantNM_000575.5(IL1A):c.54T>A (p.Asn18Lys)not specified [RCV004349601]uncertain significance2112782758112782758Humanname
15109901CV746741single nucleotide variantNM_000575.5(IL1A):c.459G>A (p.Thr153=)not provided [RCV000916427]likely benign2112779527112779527Humanname
405292479CV3192472single nucleotide variantNM_000575.5(IL1A):c.142A>G (p.Met48Val)IL1A-related disorder [RCV003929732]likely benign2112781781112781781Humanname , trait , alternate_id
405258799CV3215084single nucleotide variantNM_000575.5(IL1A):c.268C>A (p.Gln90Lys)IL1A-related disorder [RCV003942146]likely benign2112781655112781655Humanname , trait , alternate_id
405804591CV3271023single nucleotide variantNM_000575.5(IL1A):c.113T>G (p.Val38Gly)not specified [RCV004405084]uncertain significance2112781810112781810Humanname
405804593CV3271024single nucleotide variantNM_000575.5(IL1A):c.184A>G (p.Thr62Ala)not specified [RCV004405085]uncertain significance2112781739112781739Humanname
405804597CV3271026single nucleotide variantNM_000575.5(IL1A):c.262T>G (p.Leu88Val)not specified [RCV004405087]uncertain significance2112781661112781661Humanname
405804599CV3271027single nucleotide variantNM_000575.5(IL1A):c.281A>T (p.Asp94Val)not specified [RCV004405088]uncertain significance2112781642112781642Humanname
155996708CV2288539single nucleotide variantNM_000575.5(IL1A):c.517T>G (p.Ser173Ala)not specified [RCV004152066]uncertain significance2112778085112778085Humanname
155922234CV2350794single nucleotide variantNM_000575.5(IL1A):c.458C>T (p.Thr153Met)not specified [RCV004207128]likely benign2112779528112779528Humanname
156011170CV2362214single nucleotide variantNM_000575.5(IL1A):c.422A>G (p.Asn141Ser)not specified [RCV004210011]uncertain significance2112779564112779564Humanname
156307721CV2369809single nucleotide variantNM_000575.5(IL1A):c.308A>T (p.Asp103Val)not specified [RCV004215196]uncertain significance2112781615112781615Humanname
405288138CV3200559single nucleotide variantNM_000575.5(IL1A):c.340G>T (p.Ala114Ser)IL1A-related disorder [RCV003982272]benign2112779646112779646Humanname , trait , alternate_id
405266122CV3215906single nucleotide variantNM_000575.5(IL1A):c.325A>G (p.Ile109Val)IL1A-related disorder [RCV003947039]uncertain significance2112779661112779661Humanname , trait , alternate_id
405804601CV3271028single nucleotide variantNM_000575.5(IL1A):c.343C>A (p.Pro115Thr)not specified [RCV004405089]uncertain significance2112779643112779643Humanname
405804602CV3271029single nucleotide variantNM_000575.5(IL1A):c.397G>A (p.Glu133Lys)not specified [RCV004405090]uncertain significance2112779589112779589Humanname
405804604CV3271030single nucleotide variantNM_000575.5(IL1A):c.397G>C (p.Glu133Gln)not specified [RCV004405091]likely benign2112779589112779589Humanname
405804606CV3271031single nucleotide variantNM_000575.5(IL1A):c.539T>A (p.Ile180Asn)not specified [RCV004405092]uncertain significance2112778063112778063Humanname
405804608CV3271032single nucleotide variantNM_000575.5(IL1A):c.631C>T (p.Pro211Ser)not specified [RCV004405093]uncertain significance2112775252112775252Humanname
405804610CV3271033single nucleotide variantNM_000575.5(IL1A):c.734C>A (p.Ala245Asp)not specified [RCV004405094]uncertain significance2112775149112775149Humanname
407515761CV3444541single nucleotide variantNM_000575.5(IL1A):c.426A>T (p.Gln142His)not specified [RCV004627990]uncertain significance2112779560112779560Humanname
407515765CV3444542single nucleotide variantNM_000575.5(IL1A):c.443A>C (p.Asn148Thr)not specified [RCV004627991]uncertain significance2112779543112779543Humanname
597793152CV3686392single nucleotide variantNM_000575.5(IL1A):c.362A>G (p.Asn121Ser)not specified [RCV004934110]uncertain significance2112779624112779624Humanname
597793155CV3686393single nucleotide variantNM_000575.5(IL1A):c.713C>T (p.Ala238Val)not specified [RCV004934111]uncertain significance2112775170112775170Humanname
597793157CV3686394single nucleotide variantNM_000575.5(IL1A):c.566C>T (p.Thr189Ile)not specified [RCV004934112]uncertain significance2112778036112778036Humanname
15183639CV707675single nucleotide variantNM_000575.5(IL1A):c.412G>A (p.Asp138Asn)not provided [RCV000974923]benign2112779574112779574Humanname
15116088CV707676single nucleotide variantNM_000575.5(IL1A):c.373A>G (p.Asn125Asp)not provided [RCV000961974]likely benign2112779613112779613Humanname