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Variants search result for Homo sapiens
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13 records found for search term Taf12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405745357CV3331396single nucleotide variantNM_005644.4(TAF12):c.68C>G (p.Ala23Gly)not specified [RCV004466307]uncertain significance12862201428622014Humanname
597781760CV3615461single nucleotide variantNM_005644.4(TAF12):c.53T>C (p.Ile18Thr)not specified [RCV004874149]uncertain significance12862202928622029Humanname
156088978CV2241442single nucleotide variantNM_005644.4(TAF12):c.113T>C (p.Val38Ala)not specified [RCV004104354]uncertain significance12862196928621969Humanname
156070233CV2316913single nucleotide variantNM_005644.4(TAF12):c.101G>A (p.Ser34Asn)not specified [RCV004174428]uncertain significance12862198128621981Humanname
405745332CV3331393single nucleotide variantNM_005644.4(TAF12):c.119T>C (p.Ile40Thr)not specified [RCV004466304]uncertain significance12862196328621963Humanname
405745341CV3331394single nucleotide variantNM_005644.4(TAF12):c.146G>A (p.Arg49His)not specified [RCV004466305]uncertain significance12862193628621936Humanname
598182023CV3919869single nucleotide variantNM_005644.4(TAF12):c.109G>A (p.Val37Met)not specified [RCV005286854]uncertain significance12862197328621973Humanname
156379675CV2217936single nucleotide variantNM_005644.4(TAF12):c.433A>G (p.Thr145Ala)not specified [RCV004086392]uncertain significance12860538928605389Humanname
156358073CV2250860single nucleotide variantNM_005644.4(TAF12):c.467G>A (p.Arg156Gln)not specified [RCV004123454]uncertain significance12860355828603558Humanname
405745349CV3331395single nucleotide variantNM_005644.4(TAF12):c.410G>A (p.Arg137Gln)not specified [RCV004466306]uncertain significance12860541228605412Humanname
407506330CV3478533single nucleotide variantNM_005644.4(TAF12):c.398C>G (p.Ser133Cys)not specified [RCV004671087]uncertain significance12860542428605424Humanname
407530426CV3478534single nucleotide variantNM_005644.4(TAF12):c.406A>G (p.Ile136Val)not specified [RCV004681901]uncertain significance12860541628605416Humanname
598182026CV3919870single nucleotide variantNM_005644.4(TAF12):c.455T>C (p.Met152Thr)not specified [RCV005286855]uncertain significance12860357028603570Humanname