High-throughput functional analysis of PALB2 variants
收藏NIAID Data Ecosystem2026-05-02 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP488900
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资源简介：
Genetic testing of cancer susceptibility genes frequently reveals missense variants of uncertain significance (VUS) for which the impact on protein function and cancer risk are unclear. Determining the functional impact of these missense VUS can be essential for the clinical interpretation of PALB2 missense VUS and clinical management of carriers.
创建时间：
2024-12-31
