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72 records found for search term Tle1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8651373CV127948single nucleotide variantNM_005077.4(TLE1):c.594+5386A>GLung cancer [RCV000108435]uncertain significance98162796281627962Humanname
15193549CV701065single nucleotide variantNM_005077.5(TLE1):c.63T>C (p.Thr21=)not provided [RCV000955403]benign98168739681687396Humanname
329391887CV2453211single nucleotide variantNM_005077.5(TLE1):c.22C>T (p.Pro8Ser)not specified [RCV004279581]uncertain significance98168821981688219Humanname
156028632CV2195844single nucleotide variantNM_005077.5(TLE1):c.48G>T (p.Gln16His)not specified [RCV004076185]uncertain significance98168741181687411Humanname
407520754CV3475798single nucleotide variantNM_005077.5(TLE1):c.52T>C (p.Phe18Leu)not specified [RCV004677058]uncertain significance98168740781687407Humanname
407520766CV3475803single nucleotide variantNM_005077.5(TLE1):c.38C>T (p.Ala13Val)not specified [RCV004677062]uncertain significance98168742181687421Humanname
597774735CV3610225single nucleotide variantNM_005077.5(TLE1):c.54C>G (p.Phe18Leu)not specified [RCV004872374]uncertain significance98168740581687405Humanname
598176909CV3924431single nucleotide variantNM_005077.5(TLE1):c.56A>G (p.Lys19Arg)not specified [RCV005285730]uncertain significance98168740381687403Humanname
401734931CV2706589single nucleotide variantNM_005077.5(TLE1):c.155G>A (p.Ser52Asn)not specified [RCV004319174]uncertain significance98168586781685867Humanname
401911020CV2826165single nucleotide variantNM_005077.5(TLE1):c.1482C>T (p.Asn494=)not provided [RCV003425693]likely benign98159312481593124Humanname
405769967CV3346153single nucleotide variantNM_005077.5(TLE1):c.1332T>C (p.Pro444=)not specified [RCV004470115]likely benign98159327481593274Humanname
156168276CV2279982single nucleotide variantNM_005077.5(TLE1):c.517G>A (p.Gly173Arg)not specified [RCV004146348]uncertain significance98163415781634157Humanname
156325282CV2335222single nucleotide variantNM_005077.5(TLE1):c.779C>T (p.Pro260Leu)not specified [RCV004186794]uncertain significance98161612181616121Humanname
156105905CV2400404single nucleotide variantNM_005077.5(TLE1):c.497C>T (p.Ala166Val)not specified [RCV004244453]uncertain significance98163417781634177Humanname
329367577CV2427451single nucleotide variantNM_005077.5(TLE1):c.773C>T (p.Ser258Phe)not specified [RCV004248301]uncertain significance98161612781616127Humanname
401877918CV2786860single nucleotide variantNM_005077.5(TLE1):c.887C>T (p.Ser296Phe)not specified [RCV004366014]uncertain significance98161601381616013Humanname
405769992CV3346157single nucleotide variantNM_005077.5(TLE1):c.640C>T (p.Arg214Cys)not specified [RCV004470119]uncertain significance98162051281620512Humanname
405769998CV3346158single nucleotide variantNM_005077.5(TLE1):c.956C>T (p.Thr319Ile)not specified [RCV004470120]uncertain significance98161348481613484Humanname
407520746CV3475796single nucleotide variantNM_005077.5(TLE1):c.424C>T (p.Pro142Ser)not specified [RCV004677056]uncertain significance98163425081634250Humanname
407520750CV3475797single nucleotide variantNM_005077.5(TLE1):c.820G>A (p.Asp274Asn)not specified [RCV004677057]uncertain significance98161608081616080Humanname
407520757CV3475799single nucleotide variantNM_005077.5(TLE1):c.935C>T (p.Thr312Met)not specified [RCV004677059]uncertain significance98161350581613505Humanname
407520760CV3475801single nucleotide variantNM_005077.5(TLE1):c.584A>G (p.Glu195Gly)not specified [RCV004677060]uncertain significance98163335881633358Humanname
407520763CV3475802single nucleotide variantNM_005077.5(TLE1):c.318G>C (p.Gln106His)not specified [RCV004677061]uncertain significance98165226881652268Humanname
597774746CV3610227single nucleotide variantNM_005077.5(TLE1):c.557A>G (p.His186Arg)not specified [RCV004872376]uncertain significance98163411781634117Humanname
597774754CV3610229single nucleotide variantNM_005077.5(TLE1):c.524C>G (p.Ser175Cys)not specified [RCV004872378]uncertain significance98163415081634150Humanname
597774758CV3610230single nucleotide variantNM_005077.5(TLE1):c.672C>G (p.Ile224Met)not specified [RCV004872379]uncertain significance98162048081620480Humanname
597774771CV3610234single nucleotide variantNM_005077.5(TLE1):c.836T>C (p.Leu279Pro)not specified [RCV004872382]uncertain significance98161606481616064Humanname
597774777CV3610235single nucleotide variantNM_005077.5(TLE1):c.652C>T (p.Pro218Ser)not specified [RCV004872383]uncertain significance98162050081620500Humanname
597774781CV3610236single nucleotide variantNM_005077.5(TLE1):c.940G>A (p.Val314Ile)not specified [RCV004872384]uncertain significance98161350081613500Humanname
598198634CV3924429single nucleotide variantNM_005077.5(TLE1):c.433C>T (p.Pro145Ser)not specified [RCV005289743]uncertain significance98163424181634241Humanname
598176917CV3924433single nucleotide variantNM_005077.5(TLE1):c.431C>T (p.Thr144Met)not specified [RCV005285731]uncertain significance98163424381634243Humanname
598198664CV3924436single nucleotide variantNM_005077.5(TLE1):c.665A>G (p.Asn222Ser)not specified [RCV005289747]uncertain significance98162048781620487Humanname
598198674CV3924438single nucleotide variantNM_005077.5(TLE1):c.482G>T (p.Ser161Ile)not specified [RCV005289748]uncertain significance98163419281634192Humanname
598176933CV3924439single nucleotide variantNM_005077.5(TLE1):c.437A>G (p.His146Arg)not specified [RCV005285734]uncertain significance98163423781634237Humanname
598198683CV3924440single nucleotide variantNM_005077.5(TLE1):c.692A>T (p.Asp231Val)not specified [RCV005289749]uncertain significance98162046081620460Humanname
155963651CV2197975single nucleotide variantNM_005077.5(TLE1):c.1668T>G (p.Ile556Met)not specified [RCV004077185]uncertain significance98159096681590966Humanname
155975081CV2211237single nucleotide variantNM_005077.5(TLE1):c.1081C>T (p.Pro361Ser)not specified [RCV004090178]uncertain significance98161194281611942Humanname
156112090CV2217990single nucleotide variantNM_005077.5(TLE1):c.2186A>G (p.Tyr729Cys)not specified [RCV004086437]uncertain significance98158446781584467Humanname
156171801CV2286759single nucleotide variantNM_005077.5(TLE1):c.1189A>G (p.Met397Val)not specified [RCV004142570]uncertain significance98161183481611834Humanname
156015123CV2298682single nucleotide variantNM_005077.5(TLE1):c.1259G>A (p.Gly420Glu)not specified [RCV004156258]uncertain significance98161029281610292Humanname
156047952CV2319198single nucleotide variantNM_005077.5(TLE1):c.1573G>A (p.Asp525Asn)not specified [RCV004178254]uncertain significance98159303381593033Humanname
156180885CV2327773single nucleotide variantNM_005077.5(TLE1):c.1913A>G (p.Asn638Ser)not specified [RCV004179119]uncertain significance98158774581587745Humanname
155929469CV2363532single nucleotide variantNM_005077.5(TLE1):c.2005G>A (p.Gly669Arg)not specified [RCV004216102]uncertain significance98158562881585628Humanname
156267669CV2371857single nucleotide variantNM_005077.5(TLE1):c.1165G>A (p.Ala389Thr)not specified [RCV004221550]uncertain significance98161185881611858Humanname
156345777CV2377749single nucleotide variantNM_005077.5(TLE1):c.1495G>A (p.Val499Met)not specified [RCV004230333]uncertain significance98159311181593111Humanname
155929339CV2389132single nucleotide variantNM_005077.5(TLE1):c.1244G>A (p.Arg415His)not specified [RCV004235463]uncertain significance98161177981611779Humanname
156222223CV2399695single nucleotide variantNM_005077.5(TLE1):c.1219G>A (p.Ala407Thr)not specified [RCV004245514]uncertain significance98161180481611804Humanname
329357711CV2427811single nucleotide variantNM_005077.5(TLE1):c.1936C>T (p.Arg646Cys)not specified [RCV004252588]uncertain significance98158772281587722Humanname
329402351CV2454170single nucleotide variantNM_005077.5(TLE1):c.1962C>G (p.His654Gln)not specified [RCV004265660]uncertain significance98158769681587696Humanname
401739298CV2673261single nucleotide variantNM_005077.5(TLE1):c.1207G>A (p.Ala403Thr)not specified [RCV004286064]uncertain significance98161181681611816Humanname
401731093CV2674258single nucleotide variantNM_005077.5(TLE1):c.1820C>T (p.Thr607Ile)not specified [RCV004289143]uncertain significance98159081481590814Humanname
401733106CV2685427single nucleotide variantNM_005077.5(TLE1):c.2017G>A (p.Ala673Thr)not specified [RCV004294459]uncertain significance98158561681585616Humanname
401759524CV2712527single nucleotide variantNM_005077.5(TLE1):c.1185C>A (p.His395Gln)not specified [RCV004307865]uncertain significance98161183881611838Humanname
405769974CV3346154single nucleotide variantNM_005077.5(TLE1):c.1481A>T (p.Asn494Ile)not specified [RCV004470116]uncertain significance98159312581593125Humanname
405769980CV3346155single nucleotide variantNM_005077.5(TLE1):c.1544C>T (p.Pro515Leu)not specified [RCV004470117]uncertain significance98159306281593062Humanname
405769985CV3346156single nucleotide variantNM_005077.5(TLE1):c.2011T>C (p.Trp671Arg)not specified [RCV004470118]uncertain significance98158562281585622Humanname
407458469CV3475800single nucleotide variantNM_005077.5(TLE1):c.1524G>T (p.Lys508Asn)not specified [RCV004686831]uncertain significance98159308281593082Humanname
597774731CV3610224single nucleotide variantNM_005077.5(TLE1):c.2219C>T (p.Ser740Leu)not specified [RCV004872373]uncertain significance98158429281584292Humanname
597774740CV3610226single nucleotide variantNM_005077.5(TLE1):c.1144G>A (p.Gly382Ser)not specified [RCV004872375]uncertain significance98161187981611879Humanname
597774763CV3610231single nucleotide variantNM_005077.5(TLE1):c.1210G>A (p.Ala404Thr)not specified [RCV004872380]uncertain significance98161181381611813Humanname
597795158CV3610232single nucleotide variantNM_005077.5(TLE1):c.2224G>A (p.Val742Met)not specified [RCV004878096]uncertain significance98158428781584287Humanname
597774767CV3610233single nucleotide variantNM_005077.5(TLE1):c.1753G>A (p.Asp585Asn)not specified [RCV004872381]uncertain significance98159088181590881Humanname
597774785CV3610237single nucleotide variantNM_005077.5(TLE1):c.1426C>T (p.Arg476Cys)not specified [RCV004872385]uncertain significance98159318081593180Humanname
597774790CV3610238single nucleotide variantNM_005077.5(TLE1):c.1666A>G (p.Ile556Val)not specified [RCV004872386]uncertain significance98159096881590968Humanname
598198643CV3924430single nucleotide variantNM_005077.5(TLE1):c.1274C>T (p.Pro425Leu)not specified [RCV005289744]uncertain significance98161027781610277Humanname
598198650CV3924432single nucleotide variantNM_005077.5(TLE1):c.1129C>T (p.His377Tyr)not specified [RCV005289745]uncertain significance98161189481611894Humanname
598198658CV3924434single nucleotide variantNM_005077.5(TLE1):c.1558C>A (p.Pro520Thr)not specified [RCV005289746]uncertain significance98159304881593048Humanname
598176927CV3924437single nucleotide variantNM_005077.5(TLE1):c.1225G>T (p.Ala409Ser)not specified [RCV005285733]uncertain significance98161179881611798Humanname
598198692CV3924441single nucleotide variantNM_005077.5(TLE1):c.1175C>T (p.Ala392Val)not specified [RCV005289750]uncertain significance98161184881611848Humanname
598198700CV3924442single nucleotide variantNM_005077.5(TLE1):c.1633C>T (p.Leu545Phe)not specified [RCV005289751]uncertain significance98159100181591001Humanname
14398877CV613490single nucleotide variantNM_005077.5(TLE1):c.1621G>A (p.Asp541Asn)not provided [RCV000766218]uncertain significance98159101381591013Humanname
8626740CV81884single nucleotide variantNM_005077.4(TLE1):c.2188G>A (p.Gly730Arg)Malignant melanoma [RCV000061963]not provided98158446581584465Humanname