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Variants search result for Homo sapiens
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10 records found for search term Tiprl
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407520525CV3475722single nucleotide variantNM_152902.5(TIPRL):c.91G>A (p.Ala31Thr)not specified [RCV004676988]uncertain significance1168179168168179168Humanname
156189176CV2375496single nucleotide variantNM_152902.5(TIPRL):c.112G>A (p.Asp38Asn)not specified [RCV004226007]uncertain significance1168183909168183909Humanname
401885823CV2771410single nucleotide variantNM_152902.5(TIPRL):c.244A>G (p.Met82Val)not specified [RCV004348464]uncertain significance1168184041168184041Humanname
156172078CV2267825single nucleotide variantNM_152902.5(TIPRL):c.505A>C (p.Ser169Arg)not specified [RCV004136131]uncertain significance1168191489168191489Humanname
156037305CV2278825single nucleotide variantNM_152902.5(TIPRL):c.520G>A (p.Val174Ile)not specified [RCV004145536]uncertain significance1168196550168196550Humanname
405768876CV3345974single nucleotide variantNM_152902.5(TIPRL):c.397A>G (p.Thr133Ala)not specified [RCV004469936]uncertain significance1168191381168191381Humanname
407520529CV3475723single nucleotide variantNM_152902.5(TIPRL):c.444G>T (p.Lys148Asn)not specified [RCV004676989]uncertain significance1168191428168191428Humanname
598176756CV3924329single nucleotide variantNM_152902.5(TIPRL):c.791A>T (p.Asp264Val)not specified [RCV005285700]uncertain significance1168200018168200018Humanname
598198097CV3924330single nucleotide variantNM_152902.5(TIPRL):c.413C>A (p.Thr138Lys)not specified [RCV005289673]uncertain significance1168191397168191397Humanname
598198105CV3924331single nucleotide variantNM_152902.5(TIPRL):c.388G>A (p.Val130Ile)not specified [RCV005289674]uncertain significance1168191372168191372Humanname