WebMutation; HGNC; 11998; TP53; Simple; p.Cys176Phe (c.527G>T); ClinVar=VCV000376569; Zygosity=Unspecified (from parent cell line). Disease: … WebMar 1, 2012 · p.Cys176Phe c.527G>T 3% b, c 10% Not detected Not detected TL64 TP53 8 p.Arg273His c.818G>A 13% 69% Not detected Not detected TL71 KRAS 2 p.Gly12Cys …
Monoallelic TP53 inactivation is associated with poor prognosis in ...
WebJul 24, 2024 · Twelve genes were sequenced and analyzed using next-generation sequencing from formalin-fixed paraffin-embedded tissues. Allele frequency thresholds of 10, 5, and 3% were used for prognostic analyses. Results With a mean sequence depth of 3199-fold, 99% of CAGE were represented by at least 10 reads. WebMutation; HGNC; 11998; TP53; Simple; p.Cys176Phe (c.527G>T); ClinVar=VCV000376569; Zygosity=Unspecified (PubMed=8621251). Disease: Clear cell renal cell carcinoma (NCIt: C4033) Clear cell renal carcinoma (ORDO: Orphanet_319276) Species of origin: Homo sapiens (Human) (NCBI Taxonomy: 9606) Sex of cell: Female: … portable moho animation
Prevalence and Spectrum of - Oxford Academic
WebHGVS Genome Assembly; NC_000017.11:g.7675085C>A , CM000679.2:g.7675085C>A GRCh38: NC_000017.10:g.7578403C>A , CM000679.1:g.7578403C>A GRCh37 Web19 colorectal ca. tp53 p.cys176phe chr17:7578368 caccatcgct atctgagcag cgctcatggt gggggcagc gcctcaca caccatcgct atctgagcag cgctcatggt gggggcagc gcctcaca/c accatcgcta … Web28 RD Missense mutation ex 5, Cys176Phe/TGC TTC Mutated Disabling 29 RD Missense mutation ex 5, Ser149Phe/TCC TTC Mutated Disabling 30 RD Missense mutation ex 7, Arg248Trp/CGG TGG Mutated Disabling Abbreviations: ITAC, intestinal-type adenocarcinoma; pCR, pathologic complete remission; RD, residual disease; wt, wild type. irs audit for education credit