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Variants search result for Homo sapiens
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16 records found for search term Aldh3b1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155979722CV2339185single nucleotide variantNM_000694.4(ALDH3B1):c.25C>T (p.Arg9Trp)not specified [RCV004187220]uncertain significance116801532268015322Humanname
597705216CV3688054single nucleotide variantNM_000694.4(ALDH3B1):c.20C>T (p.Thr7Met)not specified [RCV004916865]uncertain significance116801531768015317Humanname
156181283CV2353069single nucleotide variantNM_000694.4(ALDH3B1):c.50C>T (p.Ala17Val)not specified [RCV004203553]uncertain significance116801534768015347Humanname
405782598CV3267531single nucleotide variantNM_000694.4(ALDH3B1):c.705C>T (p.Phe235=)not specified [RCV004397905]likely benign116802162768021627Humanname
598230310CV3970145single nucleotide variantNM_000694.4(ALDH3B1):c.513G>A (p.Gln171=)not specified [RCV005342229]likely benign116801974768019747Humanname
598230354CV3970156single nucleotide variantNM_000694.4(ALDH3B1):c.684G>A (p.Val228=)not specified [RCV005342238]likely benign116802160668021606Humanname
156083559CV2244483single nucleotide variantNM_000694.4(ALDH3B1):c.139G>A (p.Ala47Thr)not specified [RCV004100442]uncertain significance116801543668015436Humanname
401742614CV2673828single nucleotide variantNM_000694.4(ALDH3B1):c.1296C>T (p.Ser432=)not specified [RCV004293211]likely benign116802782868027828Humanname
405782514CV3267516single nucleotide variantNM_000694.4(ALDH3B1):c.1344G>A (p.Pro448=)not specified [RCV004397890]likely benign116802787668027876Humanname
156233055CV2346167single nucleotide variantNM_000694.4(ALDH3B1):c.982G>C (p.Glu328Gln)not specified [RCV004201626]uncertain significance116802262768022627Humanname
401739361CV2673273single nucleotide variantNM_000694.4(ALDH3B1):c.719C>T (p.Ala240Val)not specified [RCV004286074]uncertain significance116802164168021641Humanname
405782591CV3267530single nucleotide variantNM_000694.4(ALDH3B1):c.680C>T (p.Thr227Ile)not specified [RCV004397904]uncertain significance116802160268021602Humanname
597705225CV3688062single nucleotide variantNM_000694.4(ALDH3B1):c.602C>G (p.Ala201Gly)not specified [RCV004916866]uncertain significance116802152468021524Humanname
598230397CV3970166single nucleotide variantNM_000694.4(ALDH3B1):c.680C>G (p.Thr227Ser)not specified [RCV005342247]uncertain significance116802160268021602Humanname
155921149CV2212150single nucleotide variantNM_000694.4(ALDH3B1):c.1324C>T (p.Arg442Cys)not specified [RCV004089049]uncertain significance116802785668027856Humanname
401767836CV2677833single nucleotide variantNM_000694.4(ALDH3B1):c.1180C>T (p.His394Tyr)not specified [RCV004294330]uncertain significance116802607268026072Humanname