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Variants search result for Homo sapiens
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20 records found for search term Purb
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156238601CV2235814single nucleotide variantNM_033224.5(PURB):c.77G>A (p.Gly26Asp)not specified [RCV004111935]uncertain significance74488527244885272Humanname
156092542CV2300147single nucleotide variantNM_033224.5(PURB):c.65C>T (p.Ala22Val)not specified [RCV004151337]uncertain significance74488528444885284Humanname
156389741CV2380786single nucleotide variantNM_033224.5(PURB):c.32G>A (p.Gly11Asp)not specified [RCV004218348]uncertain significance74488531744885317Humanname
401781967CV2722363single nucleotide variantNM_033224.5(PURB):c.76G>A (p.Gly26Ser)not specified [RCV004322773]uncertain significance74488527344885273Humanname
155904796CV2276152single nucleotide variantNM_033224.5(PURB):c.221C>T (p.Thr74Met)not specified [RCV004141815]uncertain significance74488512844885128Humanname
156147164CV2311138single nucleotide variantNM_033224.5(PURB):c.277C>T (p.His93Tyr)not specified [RCV004165952]uncertain significance74488507244885072Humanname
597763488CV3582314single nucleotide variantNM_033224.5(PURB):c.212G>A (p.Ser71Asn)not specified [RCV004849549]uncertain significance74488513744885137Humanname
156316609CV2193080single nucleotide variantNM_033224.5(PURB):c.625G>T (p.Gly209Trp)not specified [RCV004069624]uncertain significance74488472444884724Humanname
156284937CV2317590single nucleotide variantNM_033224.5(PURB):c.641G>A (p.Gly214Asp)not specified [RCV004172537]uncertain significance74488470844884708Humanname
156184720CV2377760single nucleotide variantNM_033224.5(PURB):c.608G>T (p.Gly203Val)not specified [RCV004230343]uncertain significance74488474144884741Humanname
329358485CV2425270single nucleotide variantNM_033224.5(PURB):c.482C>T (p.Pro161Leu)not specified [RCV004250941]uncertain significance74488486744884867Humanname
401861168CV2769550single nucleotide variantNM_033224.5(PURB):c.343C>T (p.Pro115Ser)not specified [RCV004351203]uncertain significance74488500644885006Humanname
405658410CV3315176single nucleotide variantNM_033224.5(PURB):c.389A>G (p.Lys130Arg)not specified [RCV004438177]uncertain significance74488496044884960Humanname
405658413CV3315177single nucleotide variantNM_033224.5(PURB):c.641G>C (p.Gly214Ala)not specified [RCV004438178]uncertain significance74488470844884708Humanname
597763477CV3582311single nucleotide variantNM_033224.5(PURB):c.597G>C (p.Glu199Asp)not specified [RCV004849546]uncertain significance74488475244884752Humanname
597763480CV3582312single nucleotide variantNM_033224.5(PURB):c.481C>T (p.Pro161Ser)not specified [RCV004849547]uncertain significance74488486844884868Humanname
597763485CV3582313single nucleotide variantNM_033224.5(PURB):c.890G>T (p.Gly297Val)not specified [RCV004849548]uncertain significance74488445944884459Humanname
598250941CV3901897single nucleotide variantNM_033224.5(PURB):c.611C>T (p.Pro204Leu)not specified [RCV005259137]uncertain significance74488473844884738Humanname
598250951CV3901899single nucleotide variantNM_033224.5(PURB):c.628G>A (p.Gly210Ser)not specified [RCV005259139]uncertain significance74488472144884721Humanname
598250957CV3901900single nucleotide variantNM_033224.5(PURB):c.379G>A (p.Glu127Lys)not specified [RCV005259140]uncertain significance74488497044884970Humanname