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Variants search result for Homo sapiens
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61 records found for search term Crot
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15114444CV744262single nucleotide variantNM_021151.4(CROT):c.1063-8A>Gnot provided [RCV000894856]likely benign78738206687382066Humanname
407464264CV3429722single nucleotide variantNM_021151.4(CROT):c.116-1651G>Anot specified [RCV004613409]uncertain significance78735755587357555Humanname
8649519CV126093single nucleotide variantNM_001143935.1(CROT):c.1589-19A>GLung cancer [RCV000106580]uncertain significance78739271187392711Humanname
401736982CV2689537single nucleotide variantNM_021151.4(CROT):c.44A>G (p.Gln15Arg)not specified [RCV004308371]uncertain significance78734911287349112Humanname
401759511CV2701591single nucleotide variantNM_021151.4(CROT):c.91T>A (p.Ser31Thr)not specified [RCV004314016]uncertain significance78734915987349159Humanname
401774597CV2728208single nucleotide variantNM_021151.4(CROT):c.35G>A (p.Arg12Gln)not specified [RCV004324245]uncertain significance78734910387349103Humanname
407464292CV3429729single nucleotide variantNM_021151.4(CROT):c.284T>C (p.Ile95Thr)not specified [RCV004613416]uncertain significance78736143387361433Humanname
597799856CV3657648single nucleotide variantNM_021151.4(CROT):c.275A>G (p.Asp92Gly)not specified [RCV004905304]uncertain significance78736142487361424Humanname
15185242CV700267single nucleotide variantNM_021151.4(CROT):c.249G>T (p.Glu83Asp)not provided [RCV000952922]benign78736139887361398Humanname
156078086CV2248462single nucleotide variantNM_021151.4(CROT):c.920G>A (p.Gly307Asp)not specified [RCV004119596]uncertain significance78737739287377392Humanname
156207903CV2250075single nucleotide variantNM_021151.4(CROT):c.640C>A (p.Pro214Thr)not specified [RCV004116902]uncertain significance78736946887369468Humanname
156139154CV2250394single nucleotide variantNM_021151.4(CROT):c.815G>A (p.Ser272Asn)not specified [RCV004127276]uncertain significance78737589287375892Humanname
156250949CV2311260single nucleotide variantNM_021151.4(CROT):c.457C>A (p.Pro153Thr)not specified [RCV004166343]uncertain significance78736176287361762Humanname
156274248CV2320246single nucleotide variantNM_021151.4(CROT):c.776A>C (p.Asp259Ala)not specified [RCV004169863]uncertain significance78737585387375853Humanname
156051794CV2320256single nucleotide variantNM_021151.4(CROT):c.308T>C (p.Phe103Ser)not specified [RCV004178425]uncertain significance78736145787361457Humanname
156284463CV2349021single nucleotide variantNM_021151.4(CROT):c.356G>T (p.Gly119Val)not specified [RCV004203447]uncertain significance78736150587361505Humanname
156144278CV2358651single nucleotide variantNM_021151.4(CROT):c.712G>A (p.Ala238Thr)not specified [RCV004207524]uncertain significance78737568787375687Humanname
155928759CV2388977single nucleotide variantNM_021151.4(CROT):c.408G>C (p.Trp136Cys)not specified [RCV004241974]uncertain significance78736155787361557Humanname
401753259CV2674832single nucleotide variantNM_021151.4(CROT):c.755G>A (p.Arg252Gln)not specified [RCV004294106]uncertain significance78737583287375832Humanname
401771297CV2700984single nucleotide variantNM_021151.4(CROT):c.674A>T (p.His225Leu)not specified [RCV004307239]uncertain significance78737564987375649Humanname
401887002CV2771249single nucleotide variantNM_021151.4(CROT):c.311C>T (p.Ala104Val)not specified [RCV004346229]uncertain significance78736146087361460Humanname
405675343CV3239072single nucleotide variantNM_021151.4(CROT):c.367G>A (p.Glu123Lys)not specified [RCV004369954]uncertain significance78736151687361516Humanname
407464276CV3429725single nucleotide variantNM_021151.4(CROT):c.686A>T (p.His229Leu)not specified [RCV004613412]uncertain significance78737566187375661Humanname
407464284CV3429727single nucleotide variantNM_021151.4(CROT):c.983C>G (p.Ala328Gly)not specified [RCV004613414]uncertain significance78738191487381914Humanname
597799574CV3657639single nucleotide variantNM_021151.4(CROT):c.916T>C (p.Trp306Arg)not specified [RCV004905295]uncertain significance78737738887377388Humanname
597799580CV3657642single nucleotide variantNM_021151.4(CROT):c.710T>C (p.Ile237Thr)not specified [RCV004905298]uncertain significance78737568587375685Humanname
597799583CV3657643single nucleotide variantNM_021151.4(CROT):c.836A>G (p.Glu279Gly)not specified [RCV004905299]uncertain significance78737591387375913Humanname
597799587CV3657645single nucleotide variantNM_021151.4(CROT):c.502G>A (p.Val168Ile)not specified [RCV004905301]likely benign78736180787361807Humanname
598259823CV3962948single nucleotide variantNM_021151.4(CROT):c.914G>A (p.Arg305His)not specified [RCV005324857]uncertain significance78737738687377386Humanname
598259843CV3962952single nucleotide variantNM_021151.4(CROT):c.806T>A (p.Ile269Asn)not specified [RCV005324861]uncertain significance78737588387375883Humanname
155900923CV2241867single nucleotide variantNM_021151.4(CROT):c.1433A>G (p.Glu478Gly)not specified [RCV004106788]uncertain significance78739257387392573Humanname
156336018CV2273120single nucleotide variantNM_021151.4(CROT):c.1037T>G (p.Ile346Ser)not specified [RCV004137760]uncertain significance78738196887381968Humanname
155902444CV2301438single nucleotide variantNM_021151.4(CROT):c.1359G>C (p.Glu453Asp)not specified [RCV004162371]uncertain significance78739164687391646Humanname
156294579CV2321424single nucleotide variantNM_021151.4(CROT):c.1021T>C (p.Tyr341His)not specified [RCV004177409]uncertain significance78738195287381952Humanname
156190203CV2325454single nucleotide variantNM_021151.4(CROT):c.1636G>T (p.Val546Phe)not specified [RCV004179909]uncertain significance78739298587392985Humanname
156198613CV2365143single nucleotide variantNM_021151.4(CROT):c.1378G>C (p.Val460Leu)not specified [RCV004205165]uncertain significance78739166587391665Humanname
155956587CV2387318single nucleotide variantNM_021151.4(CROT):c.1112T>C (p.Ile371Thr)not specified [RCV004238406]likely benign78738212387382123Humanname
156092831CV2389624single nucleotide variantNM_021151.4(CROT):c.1240C>A (p.Leu414Ile)not specified [RCV004243682]uncertain significance78738248287382482Humanname
155927874CV2391557single nucleotide variantNM_021151.4(CROT):c.1352G>A (p.Arg451His)not specified [RCV004239938]uncertain significance78739163987391639Humanname
401735666CV2672711single nucleotide variantNM_021151.4(CROT):c.1027G>A (p.Asp343Asn)not specified [RCV004287724]uncertain significance78738195887381958Humanname
401751857CV2727431single nucleotide variantNM_021151.4(CROT):c.1534C>T (p.Leu512Phe)not specified [RCV004327520]uncertain significance78739275987392759Humanname
401894003CV2770212single nucleotide variantNM_021151.4(CROT):c.1547A>G (p.Glu516Gly)not specified [RCV004356103]uncertain significance78739277287392772Humanname
405675318CV3239067single nucleotide variantNM_021151.4(CROT):c.1120G>A (p.Glu374Lys)not specified [RCV004369949]uncertain significance78738213187382131Humanname
405675323CV3239068single nucleotide variantNM_021151.4(CROT):c.1406T>C (p.Met469Thr)not specified [RCV004369950]uncertain significance78739169387391693Humanname
405675329CV3239069single nucleotide variantNM_021151.4(CROT):c.1582C>G (p.Pro528Ala)not specified [RCV004369951]uncertain significance78739280787392807Humanname
405675334CV3239070single nucleotide variantNM_021151.4(CROT):c.1600G>A (p.Gly534Arg)not specified [RCV004369952]uncertain significance78739294987392949Humanname
405675339CV3239071single nucleotide variantNM_021151.4(CROT):c.1688A>G (p.Tyr563Cys)not specified [RCV004369953]uncertain significance78739303787393037Humanname
407464272CV3429724single nucleotide variantNM_021151.4(CROT):c.1418C>T (p.Ser473Phe)not specified [RCV004613411]uncertain significance78739170587391705Humanname
407464280CV3429726single nucleotide variantNM_021151.4(CROT):c.1661T>C (p.Val554Ala)not specified [RCV004613413]uncertain significance78739301087393010Humanname
407464288CV3429728single nucleotide variantNM_021151.4(CROT):c.1730C>G (p.Ala577Gly)not specified [RCV004613415]uncertain significance78739853587398535Humanname
597799572CV3657638single nucleotide variantNM_021151.4(CROT):c.1585C>G (p.Leu529Val)not specified [RCV004905294]uncertain significance78739281087392810Humanname
597799576CV3657640single nucleotide variantNM_021151.4(CROT):c.1190C>T (p.Ala397Val)not specified [RCV004905296]likely benign78738243287382432Humanname
597799578CV3657641single nucleotide variantNM_021151.4(CROT):c.1555C>T (p.Leu519Phe)not specified [RCV004905297]uncertain significance78739278087392780Humanname
597799589CV3657646single nucleotide variantNM_021151.4(CROT):c.1679A>G (p.His560Arg)not specified [RCV004905302]uncertain significance78739302887393028Humanname
597799591CV3657647single nucleotide variantNM_021151.4(CROT):c.1733G>C (p.Cys578Ser)not specified [RCV004905303]uncertain significance78739853887398538Humanname
597799859CV3657649single nucleotide variantNM_021151.4(CROT):c.1212T>A (p.Phe404Leu)not specified [RCV004905305]uncertain significance78738245487382454Humanname
598259828CV3962949single nucleotide variantNM_021151.4(CROT):c.1612A>T (p.Asn538Tyr)not specified [RCV005324858]uncertain significance78739296187392961Humanname
598259834CV3962950single nucleotide variantNM_021151.4(CROT):c.1673T>C (p.Met558Thr)not specified [RCV005324859]uncertain significance78739302287393022Humanname
598259838CV3962951single nucleotide variantNM_021151.4(CROT):c.1720T>C (p.Phe574Leu)not specified [RCV005324860]uncertain significance78739852587398525Humanname
598259848CV3962954single nucleotide variantNM_021151.4(CROT):c.1709G>C (p.Arg570Thr)not specified [RCV005324862]uncertain significance78739305887393058Humanname
598259854CV3962955single nucleotide variantNM_021151.4(CROT):c.1352G>C (p.Arg451Pro)not specified [RCV005324863]uncertain significance78739163987391639Humanname