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| == Mutations (SNV/INDEL) == | | == Mutations (SNV/INDEL) == |
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− | === From Cosmic Mutated in >20% === | + | === From Cosmic Mutated in >20%<ref>COSMIC (http://cancer.sanger.ac.uk/cosmic)</ref> === |
| === Mutated in 10-20% === | | === Mutated in 10-20% === |
| [[TP53]] | | [[TP53]] |
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| ==References== | | ==References== |
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− | Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in
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− | Atlas Research Network, Chin L, Meyerson M, Kucherlapati R, Park WY, Robertson
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− | landscape of chromophobe renal cell carcinoma.
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− | 3. Durinck S, Stawiski EW, Pavía-Jiménez A, Modrusan Z, Kapur P, Jaiswal BS,
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− | Zhang N, Toffessi-Tcheuyap V, Nguyen TT, Pahuja KB, Chen YJ, Saleem S, Chaudhuri
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− | S, Heldens S, Jackson M, Peña-Llopis S, Guillory J, Toy K, Ha C, Harris CJ,
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− | Holloman E, Hill HM, Stinson J, Rivers CS, Janakiraman V, Wang W, Kinch LN,
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− | Grishin NV, Haverty PM, Chow B, Gehring JS, Reeder J, Pau G, Wu TD, Margulis V,
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− | Spectrum of diverse genomic alterations define non-clear cell renal carcinoma
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− | 4. COSMIC (http://cancer.sanger.ac.uk/cosmic)
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