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Variants search result for Homo sapiens
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44 records found for search term Paqr4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155981525CV2244087single nucleotide variantNM_152341.5(PAQR4):c.8T>A (p.Phe3Tyr)not specified [RCV004108557]uncertain significance1629696822969682Humanname
617149461CV4021405single nucleotide variantNM_152341.5(PAQR4):c.33C>T (p.Asp11=)not provided [RCV005425374]likely benign1629697072969707Humanname
597718219CV3571373single nucleotide variantNM_152341.5(PAQR4):c.20C>G (p.Pro7Arg)not specified [RCV004841612]uncertain significance1629696942969694Humanname
598259705CV4001970single nucleotide variantNM_152341.5(PAQR4):c.23G>T (p.Arg8Leu)not specified [RCV005386537]uncertain significance1629696972969697Humanname
156282216CV2317369single nucleotide variantNM_152341.5(PAQR4):c.94G>A (p.Ala32Thr)not specified [RCV004172347]uncertain significance1629697682969768Humanname
156104132CV2363529single nucleotide variantNM_152341.5(PAQR4):c.65A>G (p.Asn22Ser)not specified [RCV004216099]uncertain significance1629697392969739Humanname
405771899CV3364248single nucleotide variantNM_152341.5(PAQR4):c.741C>T (p.Ser247=)not specified [RCV004502433]likely benign1629718672971867Humanname
405771905CV3364249single nucleotide variantNM_152341.5(PAQR4):c.765C>T (p.His255=)not specified [RCV004502434]likely benign1629718912971891Humanname
598259709CV4001971single nucleotide variantNM_152341.5(PAQR4):c.441G>A (p.Pro147=)not specified [RCV005386538]likely benign1629715672971567Humanname
156282401CV2318624single nucleotide variantNM_152341.5(PAQR4):c.232G>T (p.Asp78Tyr)not specified [RCV004173523]uncertain significance1629712222971222Humanname
156151584CV2369184single nucleotide variantNM_152341.5(PAQR4):c.109G>A (p.Gly37Ser)not specified [RCV004208107]uncertain significance1629697832969783Humanname
156170690CV2380620single nucleotide variantNM_152341.5(PAQR4):c.226G>C (p.Gly76Arg)not specified [RCV004218210]uncertain significance1629712162971216Humanname
405771862CV3364242single nucleotide variantNM_152341.5(PAQR4):c.212C>T (p.Pro71Leu)not specified [RCV004502427]uncertain significance1629712022971202Humanname
598259714CV4001972single nucleotide variantNM_152341.5(PAQR4):c.100A>G (p.Ser34Gly)not specified [RCV005386539]uncertain significance1629697742969774Humanname
156368821CV2193798single nucleotide variantNM_152341.5(PAQR4):c.487C>T (p.Arg163Cys)not specified [RCV004074552]uncertain significance1629716132971613Humanname
156237132CV2235639single nucleotide variantNM_152341.5(PAQR4):c.766G>A (p.Ala256Thr)not specified [RCV004111784]uncertain significance1629718922971892Humanname
156291328CV2236433single nucleotide variantNM_152341.5(PAQR4):c.481G>T (p.Gly161Cys)not specified [RCV004108107]uncertain significance1629716072971607Humanname
156162129CV2272658single nucleotide variantNM_152341.5(PAQR4):c.784C>G (p.Leu262Val)not specified [RCV004133535]uncertain significance1629719102971910Humanname
156257392CV2368917single nucleotide variantNM_152341.5(PAQR4):c.775G>A (p.Val259Met)not specified [RCV004207871]uncertain significance1629719012971901Humanname
156144132CV2383906single nucleotide variantNM_152341.5(PAQR4):c.667C>T (p.Arg223Cys)not specified [RCV004231762]uncertain significance1629717932971793Humanname
329358181CV2427968single nucleotide variantNM_152341.5(PAQR4):c.627G>A (p.Met209Ile)not specified [RCV004254351]uncertain significance1629717532971753Humanname
329367255CV2438887single nucleotide variantNM_152341.5(PAQR4):c.694C>T (p.Arg232Cys)not specified [RCV004264418]uncertain significance1629718202971820Humanname
329393291CV2449633single nucleotide variantNM_152341.5(PAQR4):c.547G>A (p.Ala183Thr)not specified [RCV004268550]uncertain significance1629716732971673Humanname
401737571CV2695835single nucleotide variantNM_152341.5(PAQR4):c.440C>T (p.Pro147Leu)not specified [RCV004308117]uncertain significance1629715662971566Humanname
401771023CV2700816single nucleotide variantNM_152341.5(PAQR4):c.502C>T (p.Pro168Ser)not specified [RCV004307093]uncertain significance1629716282971628Humanname
401746617CV2731881single nucleotide variantNM_152341.5(PAQR4):c.631G>A (p.Ala211Thr)not specified [RCV004333126]uncertain significance1629717572971757Humanname
401895859CV2769055single nucleotide variantNM_152341.5(PAQR4):c.805G>A (p.Ala269Thr)not specified [RCV004348922]uncertain significance1629719312971931Humanname
401861008CV2772330single nucleotide variantNM_152341.5(PAQR4):c.383C>T (p.Thr128Ile)not specified [RCV004353342]uncertain significance1629713732971373Humanname
401898895CV2792095single nucleotide variantNM_152341.5(PAQR4):c.638C>T (p.Ala213Val)not specified [RCV004361323]uncertain significance1629717642971764Humanname
405771869CV3364243single nucleotide variantNM_152341.5(PAQR4):c.340C>T (p.Arg114Trp)not specified [RCV004502428]uncertain significance1629713302971330Humanname
405771875CV3364244single nucleotide variantNM_152341.5(PAQR4):c.370T>C (p.Cys124Arg)not specified [RCV004502429]uncertain significance1629713602971360Humanname
405771889CV3364246single nucleotide variantNM_152341.5(PAQR4):c.524G>A (p.Arg175Gln)not specified [RCV004502431]uncertain significance1629716502971650Humanname
405771895CV3364247single nucleotide variantNM_152341.5(PAQR4):c.668G>A (p.Arg223His)not specified [RCV004502432]uncertain significance1629717942971794Humanname
407518160CV3466528single nucleotide variantNM_152341.5(PAQR4):c.623G>A (p.Arg208His)not specified [RCV004650909]uncertain significance1629717492971749Humanname
407518163CV3466529single nucleotide variantNM_152341.5(PAQR4):c.551G>A (p.Arg184His)not specified [RCV004650910]uncertain significance1629716772971677Humanname
597718191CV3571370single nucleotide variantNM_152341.5(PAQR4):c.769G>A (p.Gly257Ser)not specified [RCV004841609]uncertain significance1629718952971895Humanname
597718201CV3571371single nucleotide variantNM_152341.5(PAQR4):c.331G>T (p.Val111Leu)not specified [RCV004841610]uncertain significance1629713212971321Humanname
597718210CV3571372single nucleotide variantNM_152341.5(PAQR4):c.688C>T (p.Pro230Ser)not specified [RCV004841611]uncertain significance1629718142971814Humanname
597718228CV3571374single nucleotide variantNM_152341.5(PAQR4):c.686G>A (p.Gly229Glu)not specified [RCV004841613]uncertain significance1629718122971812Humanname
598259695CV4001968single nucleotide variantNM_152341.5(PAQR4):c.676G>A (p.Glu226Lys)not specified [RCV005386535]uncertain significance1629718022971802Humanname
598259700CV4001969single nucleotide variantNM_152341.5(PAQR4):c.548C>T (p.Ala183Val)not specified [RCV005386536]uncertain significance1629716742971674Humanname
598185065CV4001973single nucleotide variantNM_152341.5(PAQR4):c.815G>C (p.Arg272Pro)not specified [RCV005395549]likely benign1629719412971941Humanname
598259719CV4001974single nucleotide variantNM_152341.5(PAQR4):c.408C>A (p.His136Gln)not specified [RCV005386540]uncertain significance1629715342971534Humanname
598259724CV4001975single nucleotide variantNM_152341.5(PAQR4):c.702C>G (p.Asp234Glu)not specified [RCV005386541]uncertain significance1629718282971828Humanname