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Variants search result for Homo sapiens
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75 records found for search term Usp28
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156316016CV2192994single nucleotide variantNM_001346252.4(USP28):c.32C>T (p.Ala11Val)not specified [RCV004069547]uncertain significance11113875470113875470Humanname
329356700CV2430863single nucleotide variantNM_001346252.4(USP28):c.93C>G (p.Ile31Met)not specified [RCV004248065]uncertain significance11113854300113854300Humanname
401750191CV2715541single nucleotide variantNM_001346252.4(USP28):c.44A>T (p.Asp15Val)not specified [RCV004326941]uncertain significance11113875458113875458Humanname
155996575CV2288526single nucleotide variantNM_001346252.4(USP28):c.247G>T (p.Ala83Ser)not specified [RCV004152058]uncertain significance11113852522113852522Humanname
156163430CV2368469single nucleotide variantNM_001346252.4(USP28):c.274A>G (p.Ile92Val)not specified [RCV004221272]uncertain significance11113841763113841763Humanname
329379114CV2443301single nucleotide variantNM_001346252.4(USP28):c.148G>T (p.Asp50Tyr)not specified [RCV004260102]uncertain significance11113852621113852621Humanname
329353360CV2468981single nucleotide variantNM_001346252.4(USP28):c.217A>G (p.Thr73Ala)not specified [RCV004274244]uncertain significance11113852552113852552Humanname
401750468CV2715650single nucleotide variantNM_001346252.4(USP28):c.218C>G (p.Thr73Arg)not specified [RCV004327027]uncertain significance11113852551113852551Humanname
401909733CV2809861single nucleotide variantNM_001346252.4(USP28):c.1023T>G (p.Leu341=)not provided [RCV003398136]likely benign11113829233113829233Humanname
405814971CV3341808single nucleotide variantNM_001346252.4(USP28):c.109C>T (p.Pro37Ser)not specified [RCV004484694]uncertain significance11113854284113854284Humanname
405814988CV3341816single nucleotide variantNM_001346252.4(USP28):c.218C>T (p.Thr73Ile)not specified [RCV004484702]uncertain significance11113852551113852551Humanname
405814992CV3341818single nucleotide variantNM_001346252.4(USP28):c.265G>A (p.Ala89Thr)not specified [RCV004484704]uncertain significance11113852504113852504Humanname
9687057CV171497single nucleotide variantNM_001346252.4(USP28):c.571C>T (p.Leu191Phe)Prostate cancer [RCV000149276]pathogenic|uncertain significance11113834299113834299Human2name
156066499CV2323913single nucleotide variantNM_001346252.4(USP28):c.611G>A (p.Arg204Gln)not specified [RCV004176439]uncertain significance11113834259113834259Humanname
329375445CV2431524single nucleotide variantNM_001346252.4(USP28):c.619A>G (p.Thr207Ala)not specified [RCV004254683]uncertain significance11113834251113834251Humanname
401737549CV2679909single nucleotide variantNM_001346252.4(USP28):c.506A>G (p.Asn169Ser)not specified [RCV004284194]uncertain significance11113840626113840626Humanname
401898719CV2782626single nucleotide variantNM_001346252.4(USP28):c.310G>A (p.Ala104Thr)not specified [RCV004359650]uncertain significance11113841727113841727Humanname
405814998CV3341821single nucleotide variantNM_001346252.4(USP28):c.406C>T (p.Arg136Cys)not specified [RCV004484707]uncertain significance11113840726113840726Humanname
405815000CV3341822single nucleotide variantNM_001346252.4(USP28):c.592A>C (p.Asn198His)not specified [RCV004484708]uncertain significance11113834278113834278Humanname
405815004CV3341824single nucleotide variantNM_001346252.4(USP28):c.695T>C (p.Phe232Ser)not specified [RCV004484710]uncertain significance11113833484113833484Humanname
405815006CV3341825single nucleotide variantNM_001346252.4(USP28):c.696T>G (p.Phe232Leu)not specified [RCV004484711]uncertain significance11113833483113833483Humanname
407462646CV3487509single nucleotide variantNM_001346252.4(USP28):c.301G>T (p.Asp101Tyr)not specified [RCV004688031]uncertain significance11113841736113841736Humanname
597723240CV3626275single nucleotide variantNM_001346252.4(USP28):c.625A>G (p.Lys209Glu)not specified [RCV004888065]uncertain significance11113833554113833554Humanname
597798585CV3626277single nucleotide variantNM_001346252.4(USP28):c.808G>T (p.Ala270Ser)not specified [RCV004879265]uncertain significance11113831945113831945Humanname
597723255CV3626278single nucleotide variantNM_001346252.4(USP28):c.425G>C (p.Cys142Ser)not specified [RCV004888066]uncertain significance11113840707113840707Humanname
597798589CV3626280single nucleotide variantNM_001346252.4(USP28):c.639G>A (p.Met213Ile)not specified [RCV004879267]uncertain significance11113833540113833540Humanname
15156214CV712607single nucleotide variantNM_001346252.4(USP28):c.3102A>T (p.Val1034=)not provided [RCV000969071]benign11113801625113801625Humanname
156182922CV2198470single nucleotide variantNM_001346252.4(USP28):c.2264G>A (p.Arg755His)not specified [RCV004075507]likely benign11113808338113808338Humanname
155922484CV2207506single nucleotide variantNM_001346252.4(USP28):c.1223A>C (p.Lys408Thr)not specified [RCV004089977]uncertain significance11113823665113823665Humanname
155974253CV2211146single nucleotide variantNM_001346252.4(USP28):c.1719G>A (p.Met573Ile)not specified [RCV004088316]uncertain significance11113813909113813909Humanname
155976383CV2245972single nucleotide variantNM_001346252.4(USP28):c.1564A>G (p.Met522Val)not specified [RCV004113899]uncertain significance11113815282113815282Humanname
155979607CV2339158single nucleotide variantNM_001346252.4(USP28):c.2795C>T (p.Ala932Val)not specified [RCV004187198]uncertain significance11113804722113804722Humanname
156220705CV2345066single nucleotide variantNM_001346252.4(USP28):c.1402C>A (p.His468Asn)not specified [RCV004193344]uncertain significance11113817719113817719Humanname
156078267CV2351101single nucleotide variantNM_001346252.4(USP28):c.2567C>T (p.Ser856Phe)not specified [RCV004213963]uncertain significance11113806508113806508Humanname
156073632CV2365465single nucleotide variantNM_001346252.4(USP28):c.2045A>G (p.Gln682Arg)not specified [RCV004209538]uncertain significance11113809182113809182Humanname
156212377CV2378408single nucleotide variantNM_001346252.4(USP28):c.2001G>A (p.Met667Ile)not specified [RCV004226427]uncertain significance11113809226113809226Humanname
329373518CV2434279single nucleotide variantNM_001346252.4(USP28):c.2069A>G (p.Gln690Arg)not specified [RCV004251953]uncertain significance11113809158113809158Humanname
329354992CV2449200single nucleotide variantNM_001346252.4(USP28):c.2165A>G (p.Glu722Gly)not specified [RCV004264253]uncertain significance11113808437113808437Humanname
329355042CV2449237single nucleotide variantNM_001346252.4(USP28):c.2509A>T (p.Met837Leu)not specified [RCV004257376]uncertain significance11113806566113806566Humanname
329401687CV2457320single nucleotide variantNM_001346252.4(USP28):c.1556G>A (p.Arg519Gln)not specified [RCV004267162]uncertain significance11113815290113815290Humanname
401745235CV2681224single nucleotide variantNM_001346252.4(USP28):c.2023G>A (p.Val675Met)not specified [RCV004289362]uncertain significance11113809204113809204Humanname
401735146CV2706685single nucleotide variantNM_001346252.4(USP28):c.1350A>T (p.Glu450Asp)not specified [RCV004319258]uncertain significance11113817771113817771Humanname
401752690CV2707093single nucleotide variantNM_001346252.4(USP28):c.2985G>C (p.Met995Ile)not specified [RCV004321676]uncertain significance11113803221113803221Humanname
401888469CV2785009single nucleotide variantNM_001346252.4(USP28):c.2871C>A (p.Phe957Leu)not specified [RCV004355031]uncertain significance11113803851113803851Humanname
405814967CV3341806single nucleotide variantNM_001346252.4(USP28):c.1033G>A (p.Asp345Asn)not specified [RCV004484692]uncertain significance11113829223113829223Humanname
405814973CV3341809single nucleotide variantNM_001346252.4(USP28):c.1270C>G (p.Gln424Glu)not specified [RCV004484695]uncertain significance11113823618113823618Humanname
405814975CV3341810single nucleotide variantNM_001346252.4(USP28):c.1406T>C (p.Met469Thr)not specified [RCV004484696]uncertain significance11113817715113817715Humanname
405814977CV3341811single nucleotide variantNM_001346252.4(USP28):c.1472C>T (p.Thr491Ile)not specified [RCV004484697]uncertain significance11113815374113815374Humanname
405663869CV3341812single nucleotide variantNM_001346252.4(USP28):c.1667T>C (p.Ile556Thr)not specified [RCV004484698]uncertain significance11113815179113815179Humanname
405814981CV3341813single nucleotide variantNM_001346252.4(USP28):c.1790A>C (p.Asn597Thr)not specified [RCV004484699]uncertain significance11113812458113812458Humanname
405814983CV3341814single nucleotide variantNM_001346252.4(USP28):c.1829G>A (p.Arg610Gln)not specified [RCV004484700]uncertain significance11113812419113812419Humanname
405814985CV3341815single nucleotide variantNM_001346252.4(USP28):c.2060G>A (p.Arg687Gln)not specified [RCV004484701]uncertain significance11113809167113809167Humanname
405814989CV3341817single nucleotide variantNM_001346252.4(USP28):c.2216C>T (p.Ala739Val)not specified [RCV004484703]uncertain significance11113808386113808386Humanname
405814994CV3341819single nucleotide variantNM_001346252.4(USP28):c.2989G>A (p.Gly997Arg)not specified [RCV004484705]uncertain significance11113803217113803217Humanname
407462639CV3487506single nucleotide variantNM_001346252.4(USP28):c.2770A>G (p.Ile924Val)not specified [RCV004688029]uncertain significance11113804747113804747Humanname
407462642CV3487507single nucleotide variantNM_001346252.4(USP28):c.2532A>G (p.Ile844Met)not specified [RCV004688030]uncertain significance11113806543113806543Humanname
407455307CV3487508single nucleotide variantNM_001346252.4(USP28):c.1047G>C (p.Lys349Asn)not specified [RCV004685507]uncertain significance11113829209113829209Humanname
597798579CV3626272single nucleotide variantNM_001346252.4(USP28):c.2509A>G (p.Met837Val)not specified [RCV004879262]uncertain significance11113806566113806566Humanname
597798583CV3626276single nucleotide variantNM_001346252.4(USP28):c.1984A>G (p.Thr662Ala)not specified [RCV004879264]uncertain significance11113809243113809243Humanname
597798587CV3626279single nucleotide variantNM_001346252.4(USP28):c.2956G>A (p.Ala986Thr)not specified [RCV004879266]uncertain significance11113803250113803250Humanname
598275211CV3936580single nucleotide variantNM_001346252.4(USP28):c.1469G>C (p.Ser490Thr)not specified [RCV005304345]uncertain significance11113815377113815377Humanname
598203911CV3936581single nucleotide variantNM_001346252.4(USP28):c.2263C>T (p.Arg755Cys)not specified [RCV005290608]uncertain significance11113808339113808339Humanname
598203919CV3936582single nucleotide variantNM_001346252.4(USP28):c.1511C>T (p.Ser504Phe)not specified [RCV005290609]uncertain significance11113815335113815335Humanname
598275212CV3936583single nucleotide variantNM_001346252.4(USP28):c.1263T>G (p.Ile421Met)not specified [RCV005304346]uncertain significance11113823625113823625Humanname
598203926CV3936584single nucleotide variantNM_001346252.4(USP28):c.2264G>C (p.Arg755Pro)not specified [RCV005290610]uncertain significance11113808338113808338Humanname
598275214CV3936586single nucleotide variantNM_001346252.4(USP28):c.1220A>G (p.Asn407Ser)not specified [RCV005304348]likely benign11113823668113823668Humanname
156080294CV2198455single nucleotide variantNM_001346252.4(USP28):c.3310G>A (p.Val1104Ile)not specified [RCV004081983]uncertain significance11113799350113799350Humanname
156184563CV2239225single nucleotide variantNM_001346252.4(USP28):c.3268G>C (p.Glu1090Gln)not specified [RCV004112200]uncertain significance11113799392113799392Humanname
156063574CV2240165single nucleotide variantNM_001346252.4(USP28):c.3016G>A (p.Val1006Met)not specified [RCV004110923]uncertain significance11113803190113803190Humanname
156283624CV2317475single nucleotide variantNM_001346252.4(USP28):c.2999G>A (p.Arg1000Gln)not specified [RCV004172440]uncertain significance11113803207113803207Humanname
329389219CV2467196single nucleotide variantNM_001346252.4(USP28):c.3008A>T (p.Lys1003Ile)not specified [RCV004285013]uncertain significance11113803198113803198Humanname
401730114CV2700441single nucleotide variantNM_001346252.4(USP28):c.3260G>A (p.Cys1087Tyr)not specified [RCV004311084]uncertain significance11113799400113799400Humanname
401779652CV2714663single nucleotide variantNM_001346252.4(USP28):c.2998C>T (p.Arg1000Trp)not specified [RCV004320244]uncertain significance11113803208113803208Humanname
405814996CV3341820single nucleotide variantNM_001346252.4(USP28):c.3032G>A (p.Arg1011Gln)not specified [RCV004484706]uncertain significance11113803174113803174Humanname
598275210CV3936579single nucleotide variantNM_001346252.4(USP28):c.3280A>G (p.Arg1094Gly)not specified [RCV005304344]uncertain significance11113799380113799380Humanname