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32 records found for search term Btc
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155917045CV2239911single nucleotide variantNM_001729.4(BTC):c.8G>C (p.Arg3Pro)not specified [RCV004110464]likely benign47479431874794318Humanname
597784877CV3647118single nucleotide variantNM_001729.4(BTC):c.4G>C (p.Asp2His)not specified [RCV004900594]uncertain significance47479432274794322Humanname
156140734CV2212221single nucleotide variantNM_001729.4(BTC):c.16C>T (p.Arg6Trp)not specified [RCV004089105]uncertain significance47479431074794310Humanname
156348147CV2375647single nucleotide variantNM_001729.4(BTC):c.16C>G (p.Arg6Gly)not specified [RCV004226124]uncertain significance47479431074794310Humanname
401858293CV2774277single nucleotide variantNM_001729.4(BTC):c.14C>T (p.Ala5Val)not specified [RCV004347641]uncertain significance47479431274794312Humanname
405710836CV3298615single nucleotide variantNM_001729.4(BTC):c.46C>T (p.Leu16Phe)not specified [RCV004426785]uncertain significance47479428074794280Humanname
405710840CV3298616single nucleotide variantNM_001729.4(BTC):c.74T>A (p.Ile25Asn)not specified [RCV004426786]uncertain significance47477014774770147Humanname
597784854CV3647112single nucleotide variantNM_001729.4(BTC):c.65G>C (p.Gly22Ala)not specified [RCV004900588]uncertain significance47477015674770156Humanname
156245149CV2218946single nucleotide variantNM_001729.4(BTC):c.288T>G (p.Asp96Glu)not specified [RCV004087129]uncertain significance47475071374750713Humanname
597784858CV3647113single nucleotide variantNM_001729.4(BTC):c.253G>A (p.Val85Met)not specified [RCV004900589]uncertain significance47475588774755887Humanname
597784862CV3647114single nucleotide variantNM_001729.4(BTC):c.144C>A (p.Asp48Glu)not specified [RCV004900590]uncertain significance47477007774770077Humanname
598211268CV3949804single nucleotide variantNM_001729.4(BTC):c.110G>T (p.Arg37Ile)not specified [RCV005315985]uncertain significance47477011174770111Humanname
15113693CV709458single nucleotide variantNM_001729.4(BTC):c.130C>T (p.Leu44Phe)not provided [RCV000961537]benign47477009174770091Humanname
156178660CV2229396single nucleotide variantNM_001729.4(BTC):c.310T>C (p.Cys104Arg)not specified [RCV004101174]uncertain significance47475069174750691Humanname
156169840CV2247341single nucleotide variantNM_001729.4(BTC):c.474G>A (p.Met158Ile)not specified [RCV004108684]uncertain significance47474810474748104Humanname
156068445CV2270912single nucleotide variantNM_001729.4(BTC):c.317G>A (p.Arg106Lys)not specified [RCV004131951]uncertain significance47475068474750684Humanname
155960022CV2285353single nucleotide variantNM_001729.4(BTC):c.373A>C (p.Ile125Leu)not specified [RCV004139227]uncertain significance47475062874750628Humanname
156003899CV2396825single nucleotide variantNM_001729.4(BTC):c.463G>A (p.Glu155Lys)not specified [RCV004233959]uncertain significance47474811574748115Humanname
156002939CV2399607single nucleotide variantNM_001729.4(BTC):c.478A>G (p.Thr160Ala)not specified [RCV004244126]uncertain significance47474810074748100Humanname
401752851CV2703306single nucleotide variantNM_001729.4(BTC):c.328T>C (p.Phe110Leu)not specified [RCV004315661]uncertain significance47475067374750673Humanname
401762204CV2723356single nucleotide variantNM_001729.4(BTC):c.353A>G (p.Gln118Arg)not specified [RCV004329569]uncertain significance47475064874750648Humanname
401887468CV2773343single nucleotide variantNM_001729.4(BTC):c.298A>T (p.Ile100Phe)not specified [RCV004353997]uncertain significance47475070374750703Humanname
401872729CV2779981single nucleotide variantNM_001729.4(BTC):c.312T>G (p.Cys104Trp)not specified [RCV004353572]uncertain significance47475068974750689Humanname
405710821CV3298613single nucleotide variantNM_001729.4(BTC):c.409G>A (p.Gly137Ser)not specified [RCV004426783]uncertain significance47475059274750592Humanname
405710826CV3298614single nucleotide variantNM_001729.4(BTC):c.412G>T (p.Val138Phe)not specified [RCV004426784]uncertain significance47475058974750589Humanname
407500624CV3417754single nucleotide variantNM_001729.4(BTC):c.442C>T (p.Arg148Cys)not specified [RCV004607174]uncertain significance47474813674748136Humanname
407489761CV3417755single nucleotide variantNM_001729.4(BTC):c.398T>C (p.Ile133Thr)not specified [RCV004604104]uncertain significance47475060374750603Humanname
407489755CV3417756single nucleotide variantNM_001729.4(BTC):c.487A>G (p.Lys163Glu)not specified [RCV004604105]uncertain significance47474809174748091Humanname
597784866CV3647115single nucleotide variantNM_001729.4(BTC):c.421T>C (p.Cys141Arg)not specified [RCV004900591]uncertain significance47475058074750580Humanname
597784869CV3647116single nucleotide variantNM_001729.4(BTC):c.436C>T (p.Arg146Trp)not specified [RCV004900592]uncertain significance47474814274748142Humanname
598186624CV3949803single nucleotide variantNM_001729.4(BTC):c.406A>G (p.Ile136Val)not specified [RCV005311887]likely benign47475059574750595Humanname
8625843CV80967single nucleotide variantNM_001729.2(BTC):c.475G>A (p.Glu159Lys)Malignant melanoma [RCV000061045]not provided47474810374748103Humanname