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23 records found for search term Cldn18
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598242782CV3944501single nucleotide variantNM_016369.4(CLDN18):c.13A>T (p.Thr5Ser)not specified [RCV005321801]uncertain significance3138010238138010238Humanname
329352008CV2455608single nucleotide variantNM_016369.4(CLDN18):c.168G>C (p.Gln56His)not specified [RCV004276856]uncertain significance3138010393138010393Humanname
401720205CV2675808single nucleotide variantNM_016369.4(CLDN18):c.275T>C (p.Ile92Thr)not specified [RCV004281823]uncertain significance3138023712138023712Humanname
401750938CV2712290single nucleotide variantNM_016369.4(CLDN18):c.242C>T (p.Ala81Val)not specified [RCV004313786]uncertain significance3138023679138023679Humanname
597782322CV3660264single nucleotide variantNM_016369.4(CLDN18):c.233C>T (p.Ala78Val)not specified [RCV004899990]uncertain significance3138023670138023670Humanname
598242776CV3944500single nucleotide variantNM_016369.4(CLDN18):c.274A>G (p.Ile92Val)not specified [RCV005321800]uncertain significance3138023711138023711Humanname
156000035CV2287337single nucleotide variantNM_016369.4(CLDN18):c.469G>A (p.Gly157Ser)not specified [RCV004146959]uncertain significance3138024690138024690Humanname
156191920CV2335955single nucleotide variantNM_016369.4(CLDN18):c.476G>A (p.Gly159Asp)not specified [RCV004189565]uncertain significance3138024697138024697Humanname
156005130CV2357630single nucleotide variantNM_016369.4(CLDN18):c.590G>A (p.Arg197Gln)not specified [RCV004202891]uncertain significance3138029883138029883Humanname
156251726CV2368874single nucleotide variantNM_016369.4(CLDN18):c.688G>A (p.Gly230Ser)not provided [RCV004695699]|not specified [RCV004207833]uncertain significance3138031043138031043Humanname
156268606CV2372063single nucleotide variantNM_016369.4(CLDN18):c.313C>T (p.Arg105Cys)not specified [RCV004221732]uncertain significance3138023750138023750Humanname
156263523CV2391714single nucleotide variantNM_016369.4(CLDN18):c.770A>G (p.Lys257Arg)not specified [RCV004241869]uncertain significance3138031125138031125Humanname
329400041CV2440427single nucleotide variantNM_016369.4(CLDN18):c.634C>G (p.His212Asp)not specified [RCV004256362]uncertain significance3138030989138030989Humanname
405685705CV3306604single nucleotide variantNM_016369.4(CLDN18):c.517G>A (p.Ala173Thr)not specified [RCV004444322]uncertain significance3138029810138029810Humanname
405685711CV3306605single nucleotide variantNM_016369.4(CLDN18):c.517G>T (p.Ala173Ser)not specified [RCV004444323]likely benign3138029810138029810Humanname
405685715CV3306606single nucleotide variantNM_016369.4(CLDN18):c.577T>A (p.Cys193Ser)not specified [RCV004444324]uncertain significance3138029870138029870Humanname
405685724CV3306608single nucleotide variantNM_016369.4(CLDN18):c.584C>T (p.Ala195Val)not specified [RCV004444326]uncertain significance3138029877138029877Humanname
405685728CV3306609single nucleotide variantNM_016369.4(CLDN18):c.748G>A (p.Glu250Lys)not specified [RCV004444327]uncertain significance3138031103138031103Humanname
407462372CV3419357single nucleotide variantNM_016369.4(CLDN18):c.575T>A (p.Met192Lys)not specified [RCV004612892]uncertain significance3138029868138029868Humanname
597782326CV3660265single nucleotide variantNM_016369.4(CLDN18):c.377T>C (p.Ile126Thr)not specified [RCV004899991]uncertain significance3138023814138023814Humanname
597782330CV3660266single nucleotide variantNM_016369.4(CLDN18):c.541G>A (p.Ala181Thr)not specified [RCV004899992]uncertain significance3138029834138029834Humanname
598242770CV3944499single nucleotide variantNM_016369.4(CLDN18):c.728G>A (p.Gly243Glu)not specified [RCV005321799]uncertain significance3138031083138031083Humanname
156193313CV2223256single nucleotide variantNM_001002026.3(CLDN18):c.107A>C (p.Tyr36Ser)not specified [RCV004105877]uncertain significance3137998975137998975Humanname