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Variants search result for Homo sapiens
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7 records found for search term Cxcl13
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598236588CV3956165single nucleotide variantNM_001371558.1(CXCL13):c.55C>T (p.Pro19Ser)not specified [RCV005320465]uncertain significance47760592077605920Humanname
156166599CV2398945single nucleotide variantNM_001371558.1(CXCL13):c.167G>A (p.Arg56His)not specified [RCV004245257]uncertain significance47760780577607805Humanname
407473306CV3419964single nucleotide variantNM_001371558.1(CXCL13):c.283A>T (p.Ser95Cys)not specified [RCV004616187]uncertain significance47761099277610992Humanname
597655145CV3661776single nucleotide variantNM_001371558.1(CXCL13):c.112G>A (p.Glu38Lys)not specified [RCV004911017]uncertain significance47760775077607750Humanname
598236583CV3956164single nucleotide variantNM_001371558.1(CXCL13):c.136C>T (p.Arg46Cys)not specified [RCV005320464]uncertain significance47760777477607774Humanname
598236592CV3956166single nucleotide variantNM_001371558.1(CXCL13):c.238C>A (p.Gln80Lys)not specified [RCV005320466]uncertain significance47761065477610654Humanname
329400261CV2437523single nucleotide variantNM_001371558.1(CXCL13):c.320A>G (p.Lys107Arg)not specified [RCV004258808]likely benign47761102977611029Humanname