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Variants search result for Homo sapiens
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26 records found for search term Pawr
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155946808CV2262451single nucleotide variantNM_002583.4(PAWR):c.5C>T (p.Ala2Val)not specified [RCV004128890]uncertain significance127969024079690240Humanname
156287150CV2334998single nucleotide variantNM_002583.4(PAWR):c.61G>C (p.Glu21Gln)not specified [RCV004182091]uncertain significance127969018479690184Humanname
597671638CV3568363single nucleotide variantNM_002583.4(PAWR):c.52G>C (p.Asp18His)not specified [RCV004836396]uncertain significance127969019379690193Humanname
598244620CV4002236single nucleotide variantNM_002583.4(PAWR):c.31G>A (p.Gly11Ser)not specified [RCV005383793]uncertain significance127969021479690214Humanname
156179480CV2288011single nucleotide variantNM_002583.4(PAWR):c.191C>T (p.Ala64Val)not specified [RCV004147775]uncertain significance127969005479690054Humanname
156053199CV2360986single nucleotide variantNM_002583.4(PAWR):c.263G>A (p.Gly88Asp)not specified [RCV004216184]uncertain significance127968998279689982Humanname
405774439CV3374794single nucleotide variantNM_002583.4(PAWR):c.148G>A (p.Ala50Thr)not specified [RCV004502853]uncertain significance127969009779690097Humanname
405774445CV3374795single nucleotide variantNM_002583.4(PAWR):c.185C>G (p.Ala62Gly)not specified [RCV004502854]uncertain significance127969006079690060Humanname
597671613CV3568360single nucleotide variantNM_002583.4(PAWR):c.112G>A (p.Gly38Ser)not specified [RCV004836393]uncertain significance127969013379690133Humanname
597671646CV3568364single nucleotide variantNM_002583.4(PAWR):c.287C>T (p.Ala96Val)not specified [RCV004836397]uncertain significance127968995879689958Humanname
598244612CV4002235single nucleotide variantNM_002583.4(PAWR):c.107C>G (p.Pro36Arg)not specified [RCV005383792]uncertain significance127969013879690138Humanname
15107908CV713757single nucleotide variantNM_002583.4(PAWR):c.1005G>T (p.Val335=)not provided [RCV000960385]benign127959262579592625Humanname
156318927CV2200412single nucleotide variantNM_002583.4(PAWR):c.334C>A (p.Pro112Thr)not specified [RCV004076732]uncertain significance127968991179689911Humanname
156375348CV2210148single nucleotide variantNM_002583.4(PAWR):c.349G>A (p.Ala117Thr)not specified [RCV004087539]uncertain significance127968989679689896Humanname
156248036CV2307092single nucleotide variantNM_002583.4(PAWR):c.382G>A (p.Glu128Lys)not specified [RCV004159576]uncertain significance127968986379689863Humanname
156166803CV2315261single nucleotide variantNM_002583.4(PAWR):c.709G>T (p.Val237Phe)not specified [RCV004167250]uncertain significance127959663379596633Humanname
156117941CV2349515single nucleotide variantNM_002583.4(PAWR):c.566G>A (p.Arg189Gln)not specified [RCV004201479]uncertain significance127962115879621158Humanname
156277412CV2352043single nucleotide variantNM_002583.4(PAWR):c.605A>C (p.Glu202Ala)not specified [RCV004191139]uncertain significance127962111979621119Humanname
401759547CV2701605single nucleotide variantNM_002583.4(PAWR):c.371A>T (p.Gln124Leu)not specified [RCV004314030]uncertain significance127968987479689874Humanname
405774451CV3374796single nucleotide variantNM_002583.4(PAWR):c.299G>A (p.Arg100Gln)not specified [RCV004502855]uncertain significance127968994679689946Humanname
405774457CV3374797single nucleotide variantNM_002583.4(PAWR):c.331G>A (p.Glu111Lys)not specified [RCV004502856]uncertain significance127968991479689914Humanname
405774463CV3374798single nucleotide variantNM_002583.4(PAWR):c.424C>T (p.Pro142Ser)not specified [RCV004502857]uncertain significance127968982179689821Humanname
597671622CV3568361single nucleotide variantNM_002583.4(PAWR):c.397G>A (p.Val133Ile)not specified [RCV004836394]uncertain significance127968984879689848Humanname
597671630CV3568362single nucleotide variantNM_002583.4(PAWR):c.835G>A (p.Val279Ile)not specified [RCV004836395]uncertain significance127959443079594430Humanname
597671654CV3568365single nucleotide variantNM_002583.4(PAWR):c.796A>T (p.Ser266Cys)not specified [RCV004836398]uncertain significance127959654679596546Humanname
598244602CV4002234single nucleotide variantNM_002583.4(PAWR):c.419C>T (p.Ser140Leu)not specified [RCV005383791]uncertain significance127968982679689826Humanname