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Variants search result for Homo sapiens
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10 records found for search term Rpl32
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8577993CV112371single nucleotide variantNM_000994.3(RPL32):c.*1334A>GLung cancer [RCV000092894]uncertain significance31283476012834760Humanname
8577995CV112373single nucleotide variantNM_000994.3(RPL32):c.-6+578G>CLung cancer [RCV000092896]uncertain significance31284091612840916Humanname
405738076CV3320133single nucleotide variantNM_000994.4(RPL32):c.41A>G (p.Lys14Arg)not specified [RCV004451954]uncertain significance31284019712840197Humanname
597786189CV3594214single nucleotide variantNM_000994.4(RPL32):c.97C>T (p.Arg33Cys)not specified [RCV004854824]uncertain significance31283953012839530Humanname
401721488CV2709982single nucleotide variantNM_000994.4(RPL32):c.228G>C (p.Lys76Asn)not specified [RCV004315049]uncertain significance31283939912839399Humanname
401775493CV2710589single nucleotide variantNM_000994.4(RPL32):c.224G>A (p.Arg75Gln)not specified [RCV004319506]uncertain significance31283940312839403Humanname
405738063CV3320131single nucleotide variantNM_000994.4(RPL32):c.136C>A (p.Arg46Ser)not specified [RCV004451952]uncertain significance31283949112839491Humanname
405738069CV3320132single nucleotide variantNM_000994.4(RPL32):c.197C>T (p.Thr66Ile)not specified [RCV004451953]uncertain significance31283943012839430Humanname
597786193CV3594213single nucleotide variantNM_000994.4(RPL32):c.223C>T (p.Arg75Trp)not specified [RCV004854823]uncertain significance31283940412839404Humanname
598218768CV3906357single nucleotide variantNM_000994.4(RPL32):c.172A>G (p.Ile58Val)not specified [RCV005272340]uncertain significance31283945512839455Humanname