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Variants search result for Homo sapiens
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37 records found for search term Usp50
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15127948CV714480single nucleotide variantNM_203494.5(USP50):c.186C>G (p.Leu62=)not provided [RCV000963997]benign155054464950544649Humanname
15102072CV703243single nucleotide variantNM_203494.5(USP50):c.366A>G (p.Ala122=)not provided [RCV000959220]benign155054367650543676Humanname
329382624CV2424503single nucleotide variantNM_203494.5(USP50):c.274T>G (p.Phe92Val)not specified [RCV004252390]uncertain significance155054376850543768Humanname
401771881CV2711955single nucleotide variantNM_203494.5(USP50):c.236C>G (p.Thr79Ser)not specified [RCV004309569]uncertain significance155054459950544599Humanname
597696901CV3623216single nucleotide variantNM_203494.5(USP50):c.238G>A (p.Ala80Thr)not specified [RCV004885207]uncertain significance155054459750544597Humanname
597799111CV3623221single nucleotide variantNM_203494.5(USP50):c.269C>G (p.Thr90Ser)not specified [RCV004879538]uncertain significance155054377350543773Humanname
15102067CV703242duplicationNM_203494.5(USP50):c.915dup (p.Tyr306fs)not provided [RCV000959219]benign155052981750529818Humanname
156197018CV2259228single nucleotide variantNM_203494.5(USP50):c.781A>G (p.Ile261Val)not specified [RCV004122254]uncertain significance155053873150538731Humanname
155956362CV2304023single nucleotide variantNM_203494.5(USP50):c.844G>A (p.Asp282Asn)not specified [RCV004170075]uncertain significance155052988950529889Humanname
156177558CV2331251single nucleotide variantNM_203494.5(USP50):c.333A>G (p.Ile111Met)not specified [RCV004181854]uncertain significance155054370950543709Humanname
155908917CV2354776single nucleotide variantNM_203494.5(USP50):c.556A>C (p.Asn186His)not specified [RCV004204764]uncertain significance155054115350541153Humanname
156286560CV2360931single nucleotide variantNM_203494.5(USP50):c.493T>G (p.Cys165Gly)not specified [RCV004215745]uncertain significance155054121650541216Humanname
156052757CV2386679single nucleotide variantNM_203494.5(USP50):c.842C>T (p.Thr281Met)not specified [RCV004231016]uncertain significance155052989150529891Humanname
401746524CV2695588single nucleotide variantNM_203494.5(USP50):c.365C>T (p.Ala122Val)not specified [RCV004299411]uncertain significance155054367750543677Humanname
401725235CV2726049single nucleotide variantNM_203494.5(USP50):c.370A>C (p.Thr124Pro)not specified [RCV004324406]uncertain significance155054367250543672Humanname
401878911CV2754877single nucleotide variantNM_203494.5(USP50):c.602A>T (p.Asn201Ile)not specified [RCV004341351]uncertain significance155054110750541107Humanname
401862894CV2755721single nucleotide variantNM_203494.5(USP50):c.824C>T (p.Thr275Ile)not specified [RCV004342102]uncertain significance155052990950529909Humanname
401866061CV2762509single nucleotide variantNM_203494.5(USP50):c.568G>A (p.Val190Ile)not specified [RCV004338045]uncertain significance155054114150541141Humanname
401898539CV2784539single nucleotide variantNM_203494.5(USP50):c.691G>T (p.Ala231Ser)not specified [RCV004358698]uncertain significance155053882150538821Humanname
405801145CV3338387single nucleotide variantNM_203494.5(USP50):c.365C>A (p.Ala122Glu)not specified [RCV004477586]uncertain significance155054367750543677Humanname
405801143CV3338388single nucleotide variantNM_203494.5(USP50):c.457C>T (p.Arg153Trp)not specified [RCV004477587]uncertain significance155054125250541252Humanname
405801141CV3338389single nucleotide variantNM_203494.5(USP50):c.458G>A (p.Arg153Gln)not specified [RCV004477588]uncertain significance155054125150541251Humanname
405801139CV3338390single nucleotide variantNM_203494.5(USP50):c.604G>A (p.Glu202Lys)not specified [RCV004477589]uncertain significance155054110550541105Humanname
405801137CV3338391single nucleotide variantNM_203494.5(USP50):c.691G>A (p.Ala231Thr)not specified [RCV004477590]likely benign155053882150538821Humanname
407529058CV3487702single nucleotide variantNM_203494.5(USP50):c.371C>T (p.Thr124Met)not specified [RCV004680663]likely benign155054367150543671Humanname
407529056CV3487703single nucleotide variantNM_203494.5(USP50):c.337T>G (p.Trp113Gly)not specified [RCV004680664]uncertain significance155054370550543705Humanname
597696910CV3623217single nucleotide variantNM_203494.5(USP50):c.745A>T (p.Thr249Ser)not specified [RCV004885208]uncertain significance155053876750538767Humanname
597799108CV3623218single nucleotide variantNM_203494.5(USP50):c.386A>G (p.Gln129Arg)not specified [RCV004879536]uncertain significance155054365650543656Humanname
597799110CV3623219single nucleotide variantNM_203494.5(USP50):c.866A>C (p.Asn289Thr)not specified [RCV004879537]uncertain significance155052986750529867Humanname
597696920CV3623220single nucleotide variantNM_203494.5(USP50):c.635C>T (p.Pro212Leu)not specified [RCV004885209]uncertain significance155054107450541074Humanname
597799113CV3623222single nucleotide variantNM_203494.5(USP50):c.725T>G (p.Phe242Cys)not specified [RCV004879539]uncertain significance155053878750538787Humanname
597696928CV3623223single nucleotide variantNM_203494.5(USP50):c.758C>A (p.Ala253Asp)not specified [RCV004885210]uncertain significance155053875450538754Humanname
598204558CV3932948single nucleotide variantNM_203494.5(USP50):c.311C>T (p.Ser104Leu)not specified [RCV005290711]uncertain significance155054373150543731Humanname
598238934CV3932949single nucleotide variantNM_203494.5(USP50):c.455C>T (p.Ser152Phe)not specified [RCV005296500]uncertain significance155054125450541254Humanname
598238938CV3932950single nucleotide variantNM_203494.5(USP50):c.424C>A (p.Leu142Ile)not specified [RCV005296501]uncertain significance155054361850543618Humanname
15166979CV703241single nucleotide variantNM_203494.5(USP50):c.962G>C (p.Gly321Ala)not provided [RCV000948956]benign155050081250500812Humanname
405801035CV3338386single nucleotide variantNM_203494.5(USP50):c.1000G>C (p.Ala334Pro)not specified [RCV004477585]uncertain significance155050077450500774Humanname