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10 records found for search term Ccl22
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598192776CV3939680single nucleotide variantNM_002990.5(CCL22):c.183G>A (p.Pro61=)not specified [RCV005312844]likely benign165736054657360546Humanname
405739993CV3292462single nucleotide variantNM_002990.5(CCL22):c.37G>A (p.Val13Ile)not specified [RCV004430551]likely benign165735885357358853Humanname
156223765CV2219199single nucleotide variantNM_002990.5(CCL22):c.112C>T (p.Arg38Cys)not specified [RCV004093468]uncertain significance165736047557360475Humanname
156344559CV2346114single nucleotide variantNM_002990.5(CCL22):c.142C>T (p.Arg48Cys)not specified [RCV004201577]uncertain significance165736050557360505Humanname
155927424CV2365923single nucleotide variantNM_002990.5(CCL22):c.143G>A (p.Arg48His)not specified [RCV004207537]uncertain significance165736050657360506Humanname
405739984CV3292461single nucleotide variantNM_002990.5(CCL22):c.113G>A (p.Arg38His)not specified [RCV004430550]uncertain significance165736047657360476Humanname
407454566CV3428555single nucleotide variantNM_002990.5(CCL22):c.131G>A (p.Arg44His)not specified [RCV004609901]uncertain significance165736049457360494Humanname
407491513CV3428556single nucleotide variantNM_002990.5(CCL22):c.125G>A (p.Arg42His)not specified [RCV004604763]uncertain significance165736048857360488Humanname
15167082CV703749single nucleotide variantNM_002990.5(CCL22):c.118T>C (p.Tyr40His)not provided [RCV000948979]likely benign165736048157360481Human2name
15167082CV703749single nucleotide variantNM_002990.5(CCL22):c.118T>C (p.Tyr40His)not provided [RCV000948979]likely benign165736048157360482Human2name