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Data_Sheet_1_Case Report: Identification of a Novel Pathogenic Germline TP53 Variant in a Family With Li–Fraumeni Syndrome.DOCX

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https://figshare.com/articles/dataset/Data_Sheet_1_Case_Report_Identification_of_a_Novel_Pathogenic_Germline_TP53_Variant_in_a_Family_With_Li_Fraumeni_Syndrome_DOCX/16552251
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Li–Fraumeni syndrome (LFS) is an inherited autosomal dominant disease characterized by a predisposition to many cancers. Germline pathogenic variants in TP53 are primarily responsible for LFS. By performing a targeted sequencing panel in a proband with liver carcinoma having a deceased son affected by osteosarcoma, we found the novel heterozygous frameshift variant c.645del (p.Ser215Argfs*32) in the TP53 gene. This variant co-segregated with typical LFS cancers in the family pedigree, consistent with the pathogenicity of this novel and previously undescribed TP53 variant.
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2021-09-01
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