Targeted sequencing of APC and related cancer susceptibility genes in blood DNA from a patient with familial adenomatous polyposis

This dataset contains next-generation sequencing (NGS) alignment data derived from a blood DNA sample of a patient clinically diagnosed with familial adenomatous polyposis (FAP).Sequence analysis was performed using a multi-gene cancer panel including the APC gene, which identified a pathogenic variant, c.-30266G>A, in promoter 1B of APC.The BAM file represents cleaned and aligned sequencing reads mapped to the human reference genome (GRCh37).The purpose of this submission is to provide research-accessible genomic data supporting the identification of germline variants associated with hereditary colorectal cancer syndromes.Note: This dataset is for research use only and not intended for clinical diagnosis or treatment.