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Variants search result for Homo sapiens
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50 records found for search term Bco2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329395406CV2458338single nucleotide variantNM_031938.7(BCO2):c.14T>C (p.Val5Ala)not specified [RCV004265980]uncertain significance11112175615112175615Humanname
405711167CV3225802single nucleotide variantNM_031938.7(BCO2):c.10C>T (p.Arg4Ter)HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6 [RCV003990860]uncertain significance11112175611112175611Humanname
156192084CV2206232single nucleotide variantNM_031938.7(BCO2):c.65C>T (p.Pro22Leu)not specified [RCV004080665]uncertain significance11112175666112175666Humanname
155971604CV2309318single nucleotide variantNM_031938.7(BCO2):c.47C>T (p.Thr16Ile)not specified [RCV004165478]likely benign11112175648112175648Humanname
401905741CV2809851single nucleotide variantNM_031938.7(BCO2):c.732A>C (p.Pro244=)not provided [RCV003396080]likely benign11112194751112194751Humanname
156219943CV2226049single nucleotide variantNM_031938.7(BCO2):c.167C>T (p.Pro56Leu)not specified [RCV004105201]uncertain significance11112179356112179356Humanname
405667944CV3297999single nucleotide variantNM_031938.7(BCO2):c.283G>C (p.Gly95Arg)not specified [RCV004418906]uncertain significance11112179472112179472Humanname
597737070CV3639803single nucleotide variantNM_031938.7(BCO2):c.245G>C (p.Gly82Ala)not specified [RCV004889844]uncertain significance11112179434112179434Humanname
597737080CV3639805single nucleotide variantNM_031938.7(BCO2):c.242A>G (p.Asn81Ser)not specified [RCV004889846]uncertain significance11112179431112179431Humanname
598201712CV3938683single nucleotide variantNM_031938.7(BCO2):c.157T>C (p.Cys53Arg)not specified [RCV005314291]uncertain significance11112179346112179346Humanname
598276638CV3938687single nucleotide variantNM_031938.7(BCO2):c.277G>A (p.Glu93Lys)not specified [RCV005305772]uncertain significance11112179466112179466Humanname
156076271CV2248318single nucleotide variantNM_031938.7(BCO2):c.943C>T (p.Arg315Trp)not specified [RCV004119477]uncertain significance11112200690112200690Humanname
156242750CV2306628single nucleotide variantNM_031938.7(BCO2):c.971G>A (p.Ser324Asn)not specified [RCV004157226]uncertain significance11112200718112200718Humanname
156070182CV2325060single nucleotide variantNM_031938.7(BCO2):c.712A>C (p.Met238Leu)not specified [RCV004175601]uncertain significance11112194731112194731Humanname
156346662CV2353679single nucleotide variantNM_031938.7(BCO2):c.926T>C (p.Ile309Thr)not specified [RCV004201696]uncertain significance11112200673112200673Humanname
329360060CV2446546single nucleotide variantNM_031938.7(BCO2):c.830C>G (p.Thr277Arg)not specified [RCV004251443]uncertain significance11112199792112199792Humanname
329376235CV2465394single nucleotide variantNM_031938.7(BCO2):c.418A>G (p.Ile140Val)not specified [RCV004281171]uncertain significance11112193598112193598Humanname
401768306CV2675241single nucleotide variantNM_031938.7(BCO2):c.298A>G (p.Asn100Asp)not specified [RCV004290009]uncertain significance11112193478112193478Humanname
401736973CV2679194single nucleotide variantNM_031938.7(BCO2):c.402C>G (p.Asn134Lys)not specified [RCV004285753]uncertain significance11112193582112193582Humanname
401756309CV2687083single nucleotide variantNM_031938.7(BCO2):c.550C>T (p.Arg184Trp)not specified [RCV004304401]uncertain significance11112193911112193911Humanname
401750427CV2701235single nucleotide variantNM_031938.7(BCO2):c.668C>G (p.Ala223Gly)not specified [RCV004309808]uncertain significance11112194687112194687Humanname
401878122CV2786884single nucleotide variantNM_031938.7(BCO2):c.727G>A (p.Gly243Arg)not specified [RCV004366036]uncertain significance11112194746112194746Humanname
405667949CV3298000single nucleotide variantNM_031938.7(BCO2):c.758G>A (p.Arg253Gln)not specified [RCV004418907]uncertain significance11112199720112199720Humanname
405667959CV3298002single nucleotide variantNM_031938.7(BCO2):c.992C>T (p.Thr331Met)not specified [RCV004418909]uncertain significance11112200739112200739Humanname
597737063CV3639802single nucleotide variantNM_031938.7(BCO2):c.953C>T (p.Ala318Val)not specified [RCV004889843]uncertain significance11112200700112200700Humanname
597737074CV3639804single nucleotide variantNM_031938.7(BCO2):c.985T>C (p.Cys329Arg)not specified [RCV004889845]uncertain significance11112200732112200732Humanname
597737085CV3639806single nucleotide variantNM_031938.7(BCO2):c.857A>G (p.His286Arg)not specified [RCV004889847]uncertain significance11112199819112199819Humanname
598201698CV3938679single nucleotide variantNM_031938.7(BCO2):c.654T>G (p.Ile218Met)not specified [RCV005314288]uncertain significance11112194673112194673Humanname
598201703CV3938681single nucleotide variantNM_031938.7(BCO2):c.944G>C (p.Arg315Pro)not specified [RCV005314289]uncertain significance11112200691112200691Humanname
598201716CV3938685single nucleotide variantNM_031938.7(BCO2):c.380A>G (p.Gln127Arg)not specified [RCV005314292]uncertain significance11112193560112193560Humanname
155927918CV2227414single nucleotide variantNM_031938.7(BCO2):c.1532G>A (p.Gly511Asp)not specified [RCV004092079]uncertain significance11112216236112216236Humanname
156044946CV2234347single nucleotide variantNM_031938.7(BCO2):c.1594G>C (p.Val532Leu)not specified [RCV004100577]uncertain significance11112216298112216298Humanname
155903830CV2353678single nucleotide variantNM_031938.7(BCO2):c.1060G>A (p.Val354Ile)not specified [RCV004201695]uncertain significance11112202056112202056Humanname
155918362CV2362587single nucleotide variantNM_031938.7(BCO2):c.1331C>T (p.Thr444Met)not specified [RCV004215242]uncertain significance11112213860112213860Humanname
329376104CV2465203single nucleotide variantNM_031938.7(BCO2):c.1578T>G (p.Asn526Lys)not specified [RCV004287239]uncertain significance11112216282112216282Humanname
401731889CV2690189single nucleotide variantNM_031938.7(BCO2):c.1267G>A (p.Glu423Lys)not specified [RCV004302201]uncertain significance11112213796112213796Humanname
401741522CV2697567single nucleotide variantNM_031938.7(BCO2):c.1720G>C (p.Gly574Arg)not specified [RCV004298322]uncertain significance11112217854112217854Humanname
401877560CV2761186single nucleotide variantNM_031938.7(BCO2):c.1069C>T (p.His357Tyr)not specified [RCV004341071]uncertain significance11112202065112202065Humanname
401868582CV2767280single nucleotide variantNM_031938.7(BCO2):c.1153C>G (p.Gln385Glu)not specified [RCV004349450]uncertain significance11112202149112202149Humanname
401872982CV2776390single nucleotide variantNM_031938.7(BCO2):c.1338G>T (p.Trp446Cys)not specified [RCV004355516]uncertain significance11112214767112214767Humanname
405667931CV3297996single nucleotide variantNM_031938.7(BCO2):c.1228A>T (p.Arg410Trp)not specified [RCV004418903]uncertain significance11112213757112213757Humanname
405667935CV3297997single nucleotide variantNM_031938.7(BCO2):c.1387A>G (p.Ile463Val)not specified [RCV004418904]uncertain significance11112214816112214816Humanname
405667940CV3297998single nucleotide variantNM_031938.7(BCO2):c.1459C>T (p.Arg487Trp)not specified [RCV004418905]uncertain significance11112214888112214888Humanname
598276634CV3938678single nucleotide variantNM_031938.7(BCO2):c.1415G>A (p.Arg472Gln)not specified [RCV005305768]likely benign11112214844112214844Humanname
598276635CV3938680single nucleotide variantNM_031938.7(BCO2):c.1079A>G (p.Asn360Ser)not specified [RCV005305769]uncertain significance11112202075112202075Humanname
598201707CV3938682single nucleotide variantNM_031938.7(BCO2):c.1600C>T (p.Leu534Phe)not specified [RCV005314290]uncertain significance11112216304112216304Humanname
598276636CV3938684single nucleotide variantNM_031938.7(BCO2):c.1643T>C (p.Ile548Thr)not specified [RCV005305770]uncertain significance11112217777112217777Humanname
598276639CV3938688single nucleotide variantNM_031938.7(BCO2):c.1528G>A (p.Asp510Asn)not specified [RCV005305773]uncertain significance11112216232112216232Humanname
15102122CV701558single nucleotide variantNM_031938.7(BCO2):c.1414C>T (p.Arg472Ter)not provided [RCV000959231]likely benign11112214843112214843Humanname
401867062CV2472803deletionNM_031938.7(BCO2):c.748_755del (p.Lys250fs)not provided [RCV003331500]uncertain significance11112199707112199714Humanname