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Variants search result for Homo sapiens
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71 records found for search term Bach1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329362339CV2444618single nucleotide variantNM_001186.4(BACH1):c.82C>T (p.Arg28Trp)not specified [RCV004256839]uncertain significance212932136229321362Humanname
405260763CV3204335single nucleotide variantNM_001186.4(BACH1):c.840C>T (p.Asp280=)BACH1-related disorder [RCV003944170]likely benign212932666429326664Humanname , trait , alternate_id
329361454CV2459711single nucleotide variantNM_001186.4(BACH1):c.181T>G (p.Ser61Ala)not specified [RCV004277135]uncertain significance212932146129321461Humanname
401721136CV2702281single nucleotide variantNM_001186.4(BACH1):c.190G>A (p.Val64Ile)not specified [RCV004314612]uncertain significance212932147029321470Humanname
401758939CV2705269single nucleotide variantNM_001186.4(BACH1):c.241G>T (p.Val81Phe)not specified [RCV004311963]uncertain significance212932606529326065Humanname
405287574CV3217849single nucleotide variantNM_001186.4(BACH1):c.1833T>C (p.Gly611=)BACH1-related disorder [RCV003981972]benign212934245529342455Humanname , trait , alternate_id
405691172CV3290778single nucleotide variantNM_001186.4(BACH1):c.103G>A (p.Asp35Asn)not specified [RCV004423691]uncertain significance212932138329321383Humanname
405691189CV3290781single nucleotide variantNM_001186.4(BACH1):c.211C>G (p.Leu71Val)not specified [RCV004423694]uncertain significance212932149129321491Humanname
405691195CV3290782single nucleotide variantNM_001186.4(BACH1):c.221C>G (p.Thr74Ser)not specified [RCV004423695]uncertain significance212932150129321501Humanname
405691201CV3290783single nucleotide variantNM_001186.4(BACH1):c.267G>C (p.Gln89His)not specified [RCV004423696]uncertain significance212932609129326091Humanname
407499577CV3420828single nucleotide variantNM_001186.4(BACH1):c.109A>G (p.Thr37Ala)not specified [RCV004606911]uncertain significance212932138929321389Humanname
597704219CV3634616single nucleotide variantNM_001186.4(BACH1):c.130C>T (p.Arg44Trp)not specified [RCV004886038]uncertain significance212932141029321410Humanname
598268504CV3926295single nucleotide variantNM_001186.4(BACH1):c.118G>T (p.Val40Leu)not specified [RCV005302392]uncertain significance212932139829321398Humanname
156204225CV2252469single nucleotide variantNM_001186.4(BACH1):c.853G>A (p.Ala285Thr)not specified [RCV004116589]uncertain significance212932667729326677Humanname
155996825CV2277450single nucleotide variantNM_001186.4(BACH1):c.856A>G (p.Met286Val)not specified [RCV004144853]uncertain significance212932668029326680Humanname
156307861CV2332152single nucleotide variantNM_001186.4(BACH1):c.992A>G (p.Gln331Arg)not specified [RCV004189188]uncertain significance212932681629326816Humanname
155915838CV2339220single nucleotide variantNM_001186.4(BACH1):c.569A>G (p.Gln190Arg)not specified [RCV004191461]uncertain significance212932639329326393Humanname
156134336CV2362017single nucleotide variantNM_001186.4(BACH1):c.613C>G (p.Gln205Glu)not specified [RCV004209831]uncertain significance212932643729326437Humanname
156339482CV2367568single nucleotide variantNM_001186.4(BACH1):c.629T>C (p.Met210Thr)not specified [RCV004211497]uncertain significance212932645329326453Humanname
401737478CV2679891single nucleotide variantNM_001186.4(BACH1):c.601G>T (p.Asp201Tyr)not specified [RCV004284179]uncertain significance212932642529326425Humanname
401740686CV2681495single nucleotide variantNM_001186.4(BACH1):c.943A>G (p.Ile315Val)not specified [RCV004292029]uncertain significance212932676729326767Humanname
401725590CV2697474single nucleotide variantNM_001186.4(BACH1):c.323A>C (p.Lys108Thr)not specified [RCV004297868]uncertain significance212932614729326147Humanname
405286424CV3192175single nucleotide variantNM_001186.4(BACH1):c.808T>G (p.Cys270Gly)BACH1-related disorder [RCV003924086]likely benign212932663229326632Humanname , trait , alternate_id
405278506CV3221919single nucleotide variantNM_001186.4(BACH1):c.940T>C (p.Ser314Pro)BACH1-related disorder [RCV003976467]benign212932676429326764Humanname , trait , alternate_id
405691209CV3290784single nucleotide variantNM_001186.4(BACH1):c.468A>C (p.Lys156Asn)not specified [RCV004423697]uncertain significance212932629229326292Humanname
405691214CV3290785single nucleotide variantNM_001186.4(BACH1):c.488G>A (p.Arg163Lys)not specified [RCV004423698]likely benign212932631229326312Humanname
405691218CV3290786single nucleotide variantNM_001186.4(BACH1):c.881A>T (p.Asp294Val)not specified [RCV004423699]uncertain significance212932670529326705Humanname
405691222CV3290787single nucleotide variantNM_001186.4(BACH1):c.901A>G (p.Thr301Ala)not specified [RCV004423700]uncertain significance212932672529326725Humanname
407487018CV3420849single nucleotide variantNM_001186.4(BACH1):c.433T>A (p.Cys145Ser)not specified [RCV004603684]uncertain significance212932625729326257Humanname
407487067CV3420859single nucleotide variantNM_001186.4(BACH1):c.493C>G (p.Leu165Val)not specified [RCV004603692]uncertain significance212932631729326317Humanname
597703693CV3634557single nucleotide variantNM_001186.4(BACH1):c.587C>T (p.Ser196Leu)not specified [RCV004885984]uncertain significance212932641129326411Humanname
597703778CV3634566single nucleotide variantNM_001186.4(BACH1):c.352A>G (p.Ile118Val)not specified [RCV004885993]uncertain significance212932617629326176Humanname
597703879CV3634576single nucleotide variantNM_001186.4(BACH1):c.935A>G (p.Asn312Ser)not specified [RCV004886003]uncertain significance212932675929326759Humanname
597703987CV3634587single nucleotide variantNM_001186.4(BACH1):c.713G>T (p.Arg238Ile)not specified [RCV004886014]uncertain significance212932653729326537Humanname
597704169CV3634606single nucleotide variantNM_001186.4(BACH1):c.811A>G (p.Arg271Gly)not specified [RCV004886033]uncertain significance212932663529326635Humanname
598268423CV3926262single nucleotide variantNM_001186.4(BACH1):c.928C>T (p.Pro310Ser)not specified [RCV005302375]uncertain significance212932675229326752Humanname
598234434CV3930139single nucleotide variantNM_001186.4(BACH1):c.787T>G (p.Cys263Gly)not specified [RCV005295712]uncertain significance212932661129326611Humanname
155980587CV2263671single nucleotide variantNM_001186.4(BACH1):c.1198G>A (p.Gly400Ser)not specified [RCV004135668]uncertain significance212932702229327022Humanname
155904288CV2275873single nucleotide variantNM_001186.4(BACH1):c.1692A>T (p.Arg564Ser)not specified [RCV004139533]uncertain significance212932960929329609Humanname
156283895CV2291857single nucleotide variantNM_001186.4(BACH1):c.2024G>A (p.Arg675Gln)not specified [RCV004158384]uncertain significance212934264629342646Humanname
156019571CV2301901single nucleotide variantNM_001186.4(BACH1):c.2080C>G (p.Arg694Gly)not specified [RCV004156688]uncertain significance212934270229342702Humanname
155908440CV2302430single nucleotide variantNM_001186.4(BACH1):c.2032G>A (p.Ala678Thr)not specified [RCV004161169]uncertain significance212934265429342654Humanname
156054689CV2308688single nucleotide variantNM_001186.4(BACH1):c.1295G>A (p.Arg432Gln)not specified [RCV004169019]uncertain significance212932711929327119Humanname
155970262CV2309169single nucleotide variantNM_001186.4(BACH1):c.2142G>C (p.Gln714His)not specified [RCV004171520]uncertain significance212934276429342764Humanname
156334154CV2333346single nucleotide variantNM_001186.4(BACH1):c.2023C>T (p.Arg675Trp)not specified [RCV004190060]uncertain significance212934264529342645Humanname
156126507CV2350295single nucleotide variantNM_001186.4(BACH1):c.1294C>T (p.Arg432Trp)not specified [RCV004202249]uncertain significance212932711829327118Humanname
156009967CV2362059single nucleotide variantNM_001186.4(BACH1):c.1281G>T (p.Gln427His)not specified [RCV004209870]uncertain significance212932710529327105Humanname
155965647CV2395983single nucleotide variantNM_001186.4(BACH1):c.2057G>A (p.Gly686Glu)not specified [RCV004237531]uncertain significance212934267929342679Humanname
329372597CV2428564single nucleotide variantNM_001186.4(BACH1):c.1534A>T (p.Ser512Cys)not specified [RCV004255377]uncertain significance212932735829327358Humanname
329366941CV2441993single nucleotide variantNM_001186.4(BACH1):c.1973G>A (p.Ser658Asn)not specified [RCV004262162]uncertain significance212934259529342595Humanname
329360518CV2443594single nucleotide variantNM_001186.4(BACH1):c.1115A>C (p.Asp372Ala)not specified [RCV004262416]uncertain significance212932693929326939Humanname
329393737CV2449827single nucleotide variantNM_001186.4(BACH1):c.1341A>C (p.Glu447Asp)not specified [RCV004268925]uncertain significance212932716529327165Humanname
329358158CV2453915single nucleotide variantNM_001186.4(BACH1):c.1244A>G (p.Gln415Arg)not specified [RCV004271302]uncertain significance212932706829327068Humanname
401730025CV2683910single nucleotide variantNM_001186.4(BACH1):c.1723C>T (p.Arg575Cys)not specified [RCV004284630]uncertain significance212932964029329640Humanname
401730696CV2686659single nucleotide variantNM_001186.4(BACH1):c.1021C>G (p.Gln341Glu)not specified [RCV004300071]uncertain significance212932684529326845Humanname
401771316CV2700999single nucleotide variantNM_001186.4(BACH1):c.1989A>C (p.Glu663Asp)not specified [RCV004307253]uncertain significance212934261129342611Humanname
401751704CV2706731single nucleotide variantNM_001186.4(BACH1):c.1274C>T (p.Ser425Leu)not specified [RCV004319295]uncertain significance212932709829327098Humanname
401772079CV2723044single nucleotide variantNM_001186.4(BACH1):c.1577T>C (p.Leu526Pro)not specified [RCV004327211]uncertain significance212932949429329494Humanname
401874514CV2759244single nucleotide variantNM_001186.4(BACH1):c.1318A>G (p.Ile440Val)not specified [RCV004335841]uncertain significance212932714229327142Humanname
405281243CV3190784single nucleotide variantNM_001186.4(BACH1):c.1492A>T (p.Ile498Phe)BACH1-related disorder [RCV003907218]benign212932731629327316Humanname , trait , alternate_id
405290205CV3214146single nucleotide variantNM_001186.4(BACH1):c.1087G>C (p.Glu363Gln)BACH1-related disorder [RCV003926980]uncertain significance212932691129326911Humanname , trait , alternate_id
405691179CV3290779single nucleotide variantNM_001186.4(BACH1):c.1415G>A (p.Cys472Tyr)not specified [RCV004423692]uncertain significance212932723929327239Humanname
405691184CV3290780single nucleotide variantNM_001186.4(BACH1):c.1609T>C (p.Ser537Pro)not specified [RCV004423693]uncertain significance212932952629329526Humanname
407486977CV3420839single nucleotide variantNM_001186.4(BACH1):c.1994C>T (p.Ala665Val)not specified [RCV004603676]uncertain significance212934261629342616Humanname
407499569CV3423923single nucleotide variantNM_001186.4(BACH1):c.1406C>G (p.Thr469Ser)not specified [RCV004606909]uncertain significance212932723029327230Humanname
597704093CV3634598single nucleotide variantNM_001186.4(BACH1):c.2078C>T (p.Ala693Val)not specified [RCV004886025]uncertain significance212934270029342700Humanname
597704227CV3634624single nucleotide variantNM_001186.4(BACH1):c.1602T>G (p.Ile534Met)not specified [RCV004886039]uncertain significance212932951929329519Humanname
598268449CV3926273single nucleotide variantNM_001186.4(BACH1):c.1271G>T (p.Gly424Val)not specified [RCV005302380]uncertain significance212932709529327095Humanname
598268472CV3926284single nucleotide variantNM_001186.4(BACH1):c.1364C>A (p.Thr455Lys)not specified [RCV005302385]uncertain significance212932718829327188Humanname
14689489CV621034single nucleotide variantNM_001186.4(BACH1):c.1724G>A (p.Arg575His)Cerebellar vermis hypoplasia [RCV000779630]uncertain significance212932964129329641Human1name
8637480CV92706single nucleotide variantNM_001186.3(BACH1):c.1048C>T (p.Pro350Ser)Malignant melanoma [RCV000072804]not provided212932687229326872Humanname