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Variants search result for Homo sapiens
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93 records found for search term Prss36
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407514069CV3461555single nucleotide variantNM_173502.5(PRSS36):c.25C>T (p.Leu9Phe)not specified [RCV004649050]uncertain significance163115001131150011Humanname
329400252CV2437503single nucleotide variantNM_173502.5(PRSS36):c.33G>A (p.Met11Ile)not specified [RCV004258790]likely benign163115000331150003Humanname
329374721CV2439990single nucleotide variantNM_173502.5(PRSS36):c.59C>A (p.Ala20Asp)not specified [RCV004260469]uncertain significance163114971031149710Humanname
401782715CV2697177single nucleotide variantNM_173502.5(PRSS36):c.33G>C (p.Met11Ile)not specified [RCV004302161]likely benign163115000331150003Humanname
401883433CV2785656single nucleotide variantNM_173502.5(PRSS36):c.32T>C (p.Met11Thr)not specified [RCV004363154]uncertain significance163115000431150004Humanname
155945085CV2237932single nucleotide variantNM_173502.5(PRSS36):c.220G>A (p.Gly74Ser)not specified [RCV004109151]uncertain significance163114912531149125Humanname
156187395CV2292461single nucleotide variantNM_173502.5(PRSS36):c.176C>T (p.Pro59Leu)not specified [RCV004150250]uncertain significance163114916931149169Humanname
401759766CV2707141single nucleotide variantNM_173502.5(PRSS36):c.170C>A (p.Thr57Asn)not specified [RCV004315506]uncertain significance163114917531149175Humanname
401881443CV2759417single nucleotide variantNM_173502.5(PRSS36):c.118C>T (p.Arg40Cys)not specified [RCV004338417]uncertain significance163114922731149227Humanname
401934467CV2807885single nucleotide variantNM_173502.5(PRSS36):c.2520G>T (p.Pro840=)not provided [RCV003411335]likely benign163113918631139186Humanname
401911613CV2807886single nucleotide variantNM_173502.5(PRSS36):c.1818G>A (p.Glu606=)not provided [RCV003426681]likely benign163114155231141552Humanname
407514073CV3461558single nucleotide variantNM_173502.5(PRSS36):c.217G>A (p.Gly73Arg)not specified [RCV004649051]uncertain significance163114912831149128Humanname
15193855CV726610single nucleotide variantNM_173502.5(PRSS36):c.220G>C (p.Gly74Arg)not provided [RCV000889060]benign163114912531149125Humanname
156231841CV2199692single nucleotide variantNM_173502.5(PRSS36):c.761G>A (p.Arg254His)not specified [RCV004072428]uncertain significance163114379731143797Humanname
156204668CV2252496single nucleotide variantNM_173502.5(PRSS36):c.655A>G (p.Thr219Ala)not specified [RCV004118398]uncertain significance163114585431145854Humanname
401735447CV2672655single nucleotide variantNM_173502.5(PRSS36):c.640G>A (p.Gly214Ser)not specified [RCV004287676]uncertain significance163114586931145869Humanname
405654533CV3379317single nucleotide variantNM_173502.5(PRSS36):c.602T>G (p.Leu201Arg)not specified [RCV004510687]uncertain significance163114590731145907Humanname
405654536CV3379318single nucleotide variantNM_173502.5(PRSS36):c.640G>C (p.Gly214Arg)not specified [RCV004510688]uncertain significance163114586931145869Humanname
405654539CV3379319single nucleotide variantNM_173502.5(PRSS36):c.703C>T (p.Arg235Cys)not specified [RCV004510689]uncertain significance163114580631145806Humanname
405654541CV3379320single nucleotide variantNM_173502.5(PRSS36):c.704G>A (p.Arg235His)not specified [RCV004510690]uncertain significance163114580531145805Humanname
405654551CV3379323single nucleotide variantNM_173502.5(PRSS36):c.950A>G (p.Asn317Ser)not specified [RCV004510693]uncertain significance163114360831143608Humanname
407514059CV3461551single nucleotide variantNM_173502.5(PRSS36):c.571T>C (p.Trp191Arg)not specified [RCV004649046]uncertain significance163114593831145938Humanname
407514065CV3461554single nucleotide variantNM_173502.5(PRSS36):c.860G>A (p.Arg287Gln)not specified [RCV004649049]uncertain significance163114369831143698Humanname
407531320CV3461557single nucleotide variantNM_173502.5(PRSS36):c.858A>G (p.Ile286Met)not specified [RCV004657538]uncertain significance163114370031143700Humanname
597771572CV3581572single nucleotide variantNM_173502.5(PRSS36):c.757G>A (p.Gly253Ser)not specified [RCV004851366]uncertain significance163114380131143801Humanname
597771582CV3581574single nucleotide variantNM_173502.5(PRSS36):c.946G>A (p.Glu316Lys)not specified [RCV004851368]uncertain significance163114361231143612Humanname
597771620CV3581581single nucleotide variantNM_173502.5(PRSS36):c.622T>C (p.Cys208Arg)not specified [RCV004851375]uncertain significance163114588731145887Humanname
598160619CV3897831single nucleotide variantNM_173502.5(PRSS36):c.652C>G (p.Leu218Val)not specified [RCV005261172]uncertain significance163114585731145857Humanname
598161090CV3897833single nucleotide variantNM_173502.5(PRSS36):c.538G>A (p.Asp180Asn)not specified [RCV005261174]uncertain significance163114841031148410Humanname
598161064CV3897838single nucleotide variantNM_173502.5(PRSS36):c.736C>G (p.Pro246Ala)not specified [RCV005261179]uncertain significance163114382231143822Humanname
598161054CV3897840single nucleotide variantNM_173502.5(PRSS36):c.689G>T (p.Gly230Val)not specified [RCV005261181]uncertain significance163114582031145820Humanname
598161048CV3897841single nucleotide variantNM_173502.5(PRSS36):c.805C>G (p.Arg269Gly)not specified [RCV005261182]uncertain significance163114375331143753Humanname
156317177CV2203925single nucleotide variantNM_173502.5(PRSS36):c.1506G>C (p.Glu502Asp)not specified [RCV004069974]uncertain significance163114249631142496Humanname
156254990CV2209691single nucleotide variantNM_173502.5(PRSS36):c.2344G>A (p.Val782Met)not specified [RCV004093731]uncertain significance163113936231139362Humanname
155938843CV2229112single nucleotide variantNM_173502.5(PRSS36):c.1516T>G (p.Cys506Gly)not specified [RCV004098879]uncertain significance163114248631142486Humanname
156170115CV2247359single nucleotide variantNM_173502.5(PRSS36):c.2062C>T (p.Arg688Trp)not specified [RCV004108698]uncertain significance163114059731140597Humanname
156181417CV2255094single nucleotide variantNM_173502.5(PRSS36):c.2033C>T (p.Pro678Leu)not specified [RCV004115726]uncertain significance163114062631140626Humanname
156311069CV2260126single nucleotide variantNM_173502.5(PRSS36):c.1988G>A (p.Arg663His)not specified [RCV004119125]uncertain significance163114067131140671Humanname
156339459CV2271420single nucleotide variantNM_173502.5(PRSS36):c.1979A>T (p.Gln660Leu)not specified [RCV004136525]uncertain significance163114068031140680Humanname
156000328CV2287367single nucleotide variantNM_173502.5(PRSS36):c.1703G>A (p.Gly568Asp)not specified [RCV004146980]uncertain significance163114177931141779Humanname
155950812CV2302083single nucleotide variantNM_173502.5(PRSS36):c.1271C>G (p.Ala424Gly)not specified [RCV004158841]uncertain significance163114282331142823Humanname
156281719CV2317328single nucleotide variantNM_173502.5(PRSS36):c.2125G>T (p.Ala709Ser)not specified [RCV004178812]uncertain significance163114053431140534Humanname
156176745CV2327127single nucleotide variantNM_173502.5(PRSS36):c.1424T>A (p.Leu475Gln)not specified [RCV004178695]uncertain significance163114257831142578Humanname
156328945CV2332329single nucleotide variantNM_173502.5(PRSS36):c.1403G>A (p.Gly468Asp)not specified [RCV004182497]uncertain significance163114259931142599Humanname
155916374CV2366649single nucleotide variantNM_173502.5(PRSS36):c.2324C>T (p.Thr775Met)not specified [RCV004210657]uncertain significance163113938231139382Humanname
155904388CV2385493single nucleotide variantNM_173502.5(PRSS36):c.1450C>T (p.Pro484Ser)not specified [RCV004233139]uncertain significance163114255231142552Humanname
155927401CV2391334single nucleotide variantNM_173502.5(PRSS36):c.2464C>T (p.Pro822Ser)not specified [RCV004239742]uncertain significance163113924231139242Humanname
156220307CV2393709single nucleotide variantNM_173502.5(PRSS36):c.1958G>C (p.Ser653Thr)not specified [RCV004231511]uncertain significance163114070131140701Humanname
156113323CV2397030single nucleotide variantNM_173502.5(PRSS36):c.1321G>A (p.Gly441Arg)not specified [RCV004236547]uncertain significance163114277331142773Humanname
156101957CV2400097single nucleotide variantNM_173502.5(PRSS36):c.2063G>A (p.Arg688Gln)not specified [RCV004242908]uncertain significance163114059631140596Humanname
329371544CV2432007single nucleotide variantNM_173502.5(PRSS36):c.2468C>G (p.Thr823Ser)not specified [RCV004249160]uncertain significance163113923831139238Humanname
401727008CV2684429single nucleotide variantNM_173502.5(PRSS36):c.2333C>A (p.Ser778Tyr)not specified [RCV004291505]uncertain significance163113937331139373Humanname
401775319CV2710520single nucleotide variantNM_173502.5(PRSS36):c.1969C>G (p.Gln657Glu)not specified [RCV004319447]uncertain significance163114069031140690Humanname
401775486CV2710586single nucleotide variantNM_173502.5(PRSS36):c.2344G>C (p.Val782Leu)not specified [RCV004319504]uncertain significance163113936231139362Humanname
401764380CV2727926single nucleotide variantNM_173502.5(PRSS36):c.2369G>C (p.Arg790Pro)not specified [RCV004324107]uncertain significance163113933731139337Humanname
401895903CV2775817single nucleotide variantNM_173502.5(PRSS36):c.1961C>T (p.Ser654Phe)not specified [RCV004344856]uncertain significance163114069831140698Humanname
401890707CV2778306single nucleotide variantNM_173502.5(PRSS36):c.2264C>G (p.Ala755Gly)not specified [RCV004350359]uncertain significance163114031931140319Humanname
401876014CV2789265single nucleotide variantNM_173502.5(PRSS36):c.1741C>G (p.Pro581Ala)not specified [RCV004365294]uncertain significance163114174131141741Humanname
405654498CV3379305single nucleotide variantNM_173502.5(PRSS36):c.1054C>A (p.Leu352Met)not specified [RCV004510675]uncertain significance163114338831143388Humanname
405654501CV3379306single nucleotide variantNM_173502.5(PRSS36):c.1405G>A (p.Gly469Ser)not specified [RCV004510676]uncertain significance163114259731142597Humanname
405654504CV3379307single nucleotide variantNM_173502.5(PRSS36):c.1475C>A (p.Ala492Glu)not specified [RCV004510677]uncertain significance163114252731142527Humanname
405654507CV3379308single nucleotide variantNM_173502.5(PRSS36):c.1667G>A (p.Gly556Glu)not specified [RCV004510678]uncertain significance163114181531141815Humanname
405654510CV3379309single nucleotide variantNM_173502.5(PRSS36):c.1673A>C (p.Tyr558Ser)not specified [RCV004510679]uncertain significance163114180931141809Humanname
405654513CV3379310single nucleotide variantNM_173502.5(PRSS36):c.1739C>A (p.Pro580His)not specified [RCV004510680]uncertain significance163114174331141743Humanname
405654516CV3379311single nucleotide variantNM_173502.5(PRSS36):c.1838G>A (p.Arg613Gln)not specified [RCV004510681]uncertain significance163114153231141532Humanname
405654519CV3379312single nucleotide variantNM_173502.5(PRSS36):c.1840G>A (p.Val614Ile)not specified [RCV004510682]uncertain significance163114153031141530Humanname
405654522CV3379313single nucleotide variantNM_173502.5(PRSS36):c.2005C>T (p.Arg669Trp)not specified [RCV004510683]uncertain significance163114065431140654Humanname
405654525CV3379314single nucleotide variantNM_173502.5(PRSS36):c.2065G>T (p.Val689Leu)not specified [RCV004510684]uncertain significance163114059431140594Humanname
405654528CV3379315single nucleotide variantNM_173502.5(PRSS36):c.2318A>G (p.Gln773Arg)not specified [RCV004510685]uncertain significance163113938831139388Humanname
407514062CV3461553single nucleotide variantNM_173502.5(PRSS36):c.1832G>A (p.Gly611Asp)not specified [RCV004649048]uncertain significance163114153831141538Humanname
407531318CV3461556single nucleotide variantNM_173502.5(PRSS36):c.1051G>A (p.Ala351Thr)not specified [RCV004657537]uncertain significance163114339131143391Humanname
407531322CV3461559single nucleotide variantNM_173502.5(PRSS36):c.2203C>G (p.Arg735Gly)not specified [RCV004657539]uncertain significance163114038031140380Humanname
407514076CV3461560single nucleotide variantNM_173502.5(PRSS36):c.1298A>G (p.His433Arg)not specified [RCV004649052]uncertain significance163114279631142796Humanname
597771567CV3581571single nucleotide variantNM_173502.5(PRSS36):c.1211C>T (p.Ser404Leu)not specified [RCV004851365]uncertain significance163114288331142883Humanname
597771589CV3581575single nucleotide variantNM_173502.5(PRSS36):c.1921C>T (p.Pro641Ser)not specified [RCV004851369]uncertain significance163114073831140738Humanname
597771593CV3581576single nucleotide variantNM_173502.5(PRSS36):c.1333C>T (p.Arg445Cys)not specified [RCV004851370]uncertain significance163114276131142761Humanname
597771598CV3581577single nucleotide variantNM_173502.5(PRSS36):c.1240C>G (p.Leu414Val)not specified [RCV004851371]uncertain significance163114285431142854Humanname
597771603CV3581578single nucleotide variantNM_173502.5(PRSS36):c.2279A>T (p.Asn760Ile)not specified [RCV004851372]uncertain significance163114030431140304Humanname
597771610CV3581579single nucleotide variantNM_173502.5(PRSS36):c.1559G>A (p.Gly520Glu)not specified [RCV004851373]uncertain significance163114192331141923Humanname
597771615CV3581580single nucleotide variantNM_173502.5(PRSS36):c.2360A>T (p.Gln787Leu)not specified [RCV004851374]uncertain significance163113934631139346Humanname
597771626CV3581582single nucleotide variantNM_173502.5(PRSS36):c.1792G>A (p.Gly598Arg)not specified [RCV004851376]uncertain significance163114157831141578Humanname
597771636CV3581584single nucleotide variantNM_173502.5(PRSS36):c.1144C>A (p.Arg382Ser)not specified [RCV004851378]uncertain significance163114295031142950Humanname
597771642CV3581585single nucleotide variantNM_173502.5(PRSS36):c.2237C>G (p.Pro746Arg)not specified [RCV004851379]uncertain significance163114034631140346Humanname
597771646CV3581586single nucleotide variantNM_173502.5(PRSS36):c.1208C>G (p.Ala403Gly)not specified [RCV004851380]uncertain significance163114288631142886Humanname
597771653CV3581587single nucleotide variantNM_173502.5(PRSS36):c.1784C>A (p.Ala595Asp)not specified [RCV004851381]uncertain significance163114158631141586Humanname
597771658CV3581588single nucleotide variantNM_173502.5(PRSS36):c.1120C>A (p.Pro374Thr)not specified [RCV004851382]uncertain significance163114297431142974Humanname
598160614CV3897830single nucleotide variantNM_173502.5(PRSS36):c.2006G>A (p.Arg669Gln)not specified [RCV005261171]uncertain significance163114065331140653Humanname
598161095CV3897832single nucleotide variantNM_173502.5(PRSS36):c.1052C>T (p.Ala351Val)not specified [RCV005261173]uncertain significance163114339031143390Humanname
598161085CV3897834single nucleotide variantNM_173502.5(PRSS36):c.1230C>G (p.Asp410Glu)not specified [RCV005261175]uncertain significance163114286431142864Humanname
598161080CV3897835single nucleotide variantNM_173502.5(PRSS36):c.1582A>G (p.Arg528Gly)not specified [RCV005261176]uncertain significance163114190031141900Humanname
598161075CV3897836single nucleotide variantNM_173502.5(PRSS36):c.1792G>C (p.Gly598Arg)not specified [RCV005261177]uncertain significance163114157831141578Humanname
598161070CV3897837single nucleotide variantNM_173502.5(PRSS36):c.1951G>A (p.Gly651Arg)not specified [RCV005261178]uncertain significance163114070831140708Humanname
598161059CV3897839single nucleotide variantNM_173502.5(PRSS36):c.1921C>A (p.Pro641Thr)not specified [RCV005261180]uncertain significance163114073831140738Humanname