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Variants search result for Homo sapiens
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25 records found for search term Mrpl17
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156347617CV2315360single nucleotide variantNM_022061.4(MRPL17):c.4C>T (p.Arg2Trp)not specified [RCV004167334]uncertain significance1166832936683293Humanname
407525173CV3450303single nucleotide variantNM_022061.4(MRPL17):c.23C>T (p.Ala8Val)not specified [RCV004631641]uncertain significance1166832746683274Humanname
156111219CV2261715single nucleotide variantNM_022061.4(MRPL17):c.52A>T (p.Met18Leu)not specified [RCV004126016]likely benign1166832456683245Humanname
155944663CV2271869single nucleotide variantNM_022061.4(MRPL17):c.89G>A (p.Arg30Gln)not specified [RCV004130686]uncertain significance1166832086683208Humanname
156072431CV2335023single nucleotide variantNM_022061.4(MRPL17):c.32A>G (p.His11Arg)not specified [RCV004182113]uncertain significance1166832656683265Humanname
329379491CV2443432single nucleotide variantNM_022061.4(MRPL17):c.33T>A (p.His11Gln)not specified [RCV004262272]uncertain significance1166832646683264Humanname
405853044CV3393475single nucleotide variantNM_022061.4(MRPL17):c.408T>A (p.Pro136=)not provided [RCV004546205]likely benign1166822386682238Humanname
598212668CV3982831single nucleotide variantNM_022061.4(MRPL17):c.52A>G (p.Met18Val)not specified [RCV005378217]uncertain significance1166832456683245Humanname
598212674CV3982832single nucleotide variantNM_022061.4(MRPL17):c.74G>A (p.Arg25His)not specified [RCV005378218]uncertain significance1166832236683223Humanname
405771078CV3363964single nucleotide variantNM_022061.4(MRPL17):c.119A>G (p.Glu40Gly)not specified [RCV004502318]uncertain significance1166831786683178Humanname
407474399CV3450299single nucleotide variantNM_022061.4(MRPL17):c.164A>G (p.Tyr55Cys)not specified [RCV004638144]uncertain significance1166831336683133Humanname
407525170CV3450302single nucleotide variantNM_022061.4(MRPL17):c.176T>C (p.Leu59Pro)not specified [RCV004631640]uncertain significance1166828146682814Humanname
597633574CV3561095single nucleotide variantNM_022061.4(MRPL17):c.136T>C (p.Trp46Arg)not specified [RCV004830827]uncertain significance1166831616683161Humanname
598178795CV3982834single nucleotide variantNM_022061.4(MRPL17):c.271C>A (p.Gln91Lys)not specified [RCV005371825]likely benign1166823756682375Humanname
598212688CV3982835single nucleotide variantNM_022061.4(MRPL17):c.208G>A (p.Glu70Lys)not specified [RCV005378220]uncertain significance1166827826682782Humanname
598212695CV3982836single nucleotide variantNM_022061.4(MRPL17):c.292A>G (p.Lys98Glu)not specified [RCV005378221]uncertain significance1166823546682354Humanname
156281936CV2295153single nucleotide variantNM_022061.4(MRPL17):c.514A>C (p.Thr172Pro)not specified [RCV004158252]uncertain significance1166821326682132Humanname
155922787CV2340684single nucleotide variantNM_022061.4(MRPL17):c.489C>G (p.Ser163Arg)not specified [RCV004190356]uncertain significance1166821576682157Humanname
156401937CV2371203single nucleotide variantNM_022061.4(MRPL17):c.369C>G (p.Ile123Met)not specified [RCV004220942]uncertain significance1166822776682277Humanname
329359864CV2462345single nucleotide variantNM_022061.4(MRPL17):c.308G>A (p.Gly103Asp)not specified [RCV004266328]uncertain significance1166823386682338Humanname
405771171CV3363981single nucleotide variantNM_022061.4(MRPL17):c.350G>A (p.Arg117Gln)not specified [RCV004502335]uncertain significance1166822966682296Humanname
407525168CV3450300single nucleotide variantNM_022061.4(MRPL17):c.307G>A (p.Gly103Ser)not specified [RCV004631639]uncertain significance1166823396682339Humanname
407474403CV3450301single nucleotide variantNM_022061.4(MRPL17):c.314C>G (p.Thr105Arg)not specified [RCV004638145]uncertain significance1166823326682332Humanname
597637826CV3561096single nucleotide variantNM_022061.4(MRPL17):c.370G>A (p.Glu124Lys)not specified [RCV004824807]uncertain significance1166822766682276Humanname
598212681CV3982833single nucleotide variantNM_022061.4(MRPL17):c.383A>G (p.Asn128Ser)not specified [RCV005378219]uncertain significance1166822636682263Humanname