Mutations/alterations of 95 FANCD1/BRCA2 patients included in our study. The color coding for frameshift/nonsense mutations, splice donor variants, splice acceptor variants, missense variants, and finally benign alterations (*) found in patients who were not used in the risk score analysis is shown above. VUS (**) found in patients who were not used in the risk score analysis. The nucleotide numbering is based on BRCA2 transcript NM_000059.4.