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Variants search result for Homo sapiens
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37 records found for search term Gfra4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405787121CV3258346single nucleotide variantNM_022139.4(GFRA4):c.392+5G>Cnot specified [RCV004387850]uncertain significance2036609393660939Humanname
15197931CV760892single nucleotide variantNM_022139.4(GFRA4):c.637+9C>Gnot provided [RCV000912114]likely benign2036605173660517Humanname
156035607CV2282992single nucleotide variantNM_022139.4(GFRA4):c.392+24C>Anot specified [RCV004143621]likely benign2036609203660920Humanname
156079164CV2341237single nucleotide variantNM_022139.4(GFRA4):c.23C>T (p.Ala8Val)not specified [RCV004186650]likely benign2036633773663377Humanname
401772145CV2719548single nucleotide variantNM_022139.4(GFRA4):c.14T>A (p.Leu5Gln)not specified [RCV004327230]uncertain significance2036633863663386Humanname
155928869CV2224449single nucleotide variantNM_022139.4(GFRA4):c.444C>G (p.Pro148=)not specified [RCV004098048]uncertain significance2036608133660813Humanname
329373681CV2434202single nucleotide variantNM_022139.4(GFRA4):c.489C>T (p.Tyr163=)not specified [RCV004250092]uncertain significance2036607683660768Humanname
407512922CV3433046single nucleotide variantNM_022139.4(GFRA4):c.50C>T (p.Ser17Leu)not specified [RCV004626957]uncertain significance2036612863661286Humanname
156143135CV2208610single nucleotide variantNM_022139.4(GFRA4):c.128G>C (p.Arg43Pro)not specified [RCV004091130]uncertain significance2036612083661208Humanname
156168859CV2296497single nucleotide variantNM_022139.4(GFRA4):c.229C>T (p.Pro77Ser)not specified [RCV004154578]uncertain significance2036611073661107Humanname
156257116CV2369305single nucleotide variantNM_022139.4(GFRA4):c.209G>A (p.Arg70His)not specified [RCV004208216]uncertain significance2036611273661127Humanname
329376948CV2435753single nucleotide variantNM_022139.4(GFRA4):c.155G>T (p.Gly52Val)not specified [RCV004253382]uncertain significance2036611813661181Humanname
329376012CV2437927single nucleotide variantNM_022139.4(GFRA4):c.200C>G (p.Ala67Gly)not specified [RCV004263651]uncertain significance2036611363661136Humanname
401894752CV2785264single nucleotide variantNM_022139.4(GFRA4):c.283G>A (p.Glu95Lys)not specified [RCV004357030]uncertain significance2036610533661053Humanname
405786827CV3258343single nucleotide variantNM_022139.4(GFRA4):c.121C>A (p.Arg41Ser)not specified [RCV004387847]uncertain significance2036612153661215Humanname
407512927CV3433047single nucleotide variantNM_022139.4(GFRA4):c.230C>T (p.Pro77Leu)not specified [RCV004626958]uncertain significance2036611063661106Humanname
597758914CV3684207single nucleotide variantNM_022139.4(GFRA4):c.104C>G (p.Ala35Gly)not specified [RCV004925391]uncertain significance2036612323661232Humanname
597758922CV3684210single nucleotide variantNM_022139.4(GFRA4):c.179C>G (p.Pro60Arg)not specified [RCV004925393]uncertain significance2036611573661157Humanname
598250742CV3967093single nucleotide variantNM_022139.4(GFRA4):c.139G>C (p.Val47Leu)not specified [RCV005345761]uncertain significance2036611973661197Humanname
15040456CV680134single nucleotide variantNM_022139.4(GFRA4):c.244G>C (p.Ala82Pro)Fetal akinesia deformation sequence 1 [RCV000855512]uncertain significance2036610923661092Human3name
156153809CV2209473single nucleotide variantNM_022139.4(GFRA4):c.791C>T (p.Ala264Val)not specified [RCV004093616]uncertain significance2036599283659928Humanname
156347806CV2315468single nucleotide variantNM_022139.4(GFRA4):c.323C>T (p.Ser108Leu)not specified [RCV004167418]uncertain significance2036610133661013Humanname
156288363CV2327406single nucleotide variantNM_022139.4(GFRA4):c.515C>A (p.Thr172Asn)not specified [RCV004174830]uncertain significance2036606483660648Humanname
329396288CV2462486single nucleotide variantNM_022139.4(GFRA4):c.702G>C (p.Gln234His)not specified [RCV004276664]likely benign2036601853660185Humanname
401884518CV2759359single nucleotide variantNM_022139.4(GFRA4):c.458T>C (p.Leu153Pro)not specified [RCV004335941]likely benign2036607993660799Humanname
401867363CV2773421single nucleotide variantNM_022139.4(GFRA4):c.628C>T (p.Arg210Cys)not specified [RCV004354061]uncertain significance2036605353660535Humanname
405786838CV3258345single nucleotide variantNM_022139.4(GFRA4):c.346T>C (p.Ser116Pro)not specified [RCV004387849]uncertain significance2036609903660990Humanname
597705341CV3684204single nucleotide variantNM_022139.4(GFRA4):c.440C>T (p.Ala147Val)not specified [RCV004916879]likely benign2036608173660817Humanname
597758909CV3684205single nucleotide variantNM_022139.4(GFRA4):c.544C>T (p.Arg182Cys)not specified [RCV004925390]uncertain significance2036606193660619Humanname
597705351CV3684206single nucleotide variantNM_022139.4(GFRA4):c.584G>A (p.Arg195Gln)not specified [RCV004916880]uncertain significance2036605793660579Humanname
597758917CV3684208single nucleotide variantNM_022139.4(GFRA4):c.522C>G (p.Asn174Lys)not specified [RCV004925392]uncertain significance2036606413660641Humanname
597705361CV3684209single nucleotide variantNM_022139.4(GFRA4):c.749C>T (p.Ala250Val)not specified [RCV004916881]uncertain significance2036599703659970Humanname
597758927CV3684211single nucleotide variantNM_022139.4(GFRA4):c.323C>G (p.Ser108Trp)not specified [RCV004925394]uncertain significance2036610133661013Humanname
598250729CV3967091single nucleotide variantNM_022139.4(GFRA4):c.434C>G (p.Pro145Arg)not specified [RCV005345759]likely benign2036608233660823Humanname
598250736CV3967092single nucleotide variantNM_022139.4(GFRA4):c.433C>T (p.Pro145Ser)not specified [RCV005345760]uncertain significance2036608243660824Humanname
598220206CV3967094single nucleotide variantNM_022139.4(GFRA4):c.794T>C (p.Leu265Pro)not specified [RCV005340414]uncertain significance2036599253659925Humanname
598250747CV3967095single nucleotide variantNM_022139.4(GFRA4):c.611G>T (p.Gly204Val)not specified [RCV005345762]uncertain significance2036605523660552Humanname