Table 4.
Patient ID | Tissue Source (1=primary, 2=metastatic) | Germline Mutation | Somatic Mutations |
---|---|---|---|
2 | 1 | Not tested | TP53 (p.R273C) |
2 | 2 | Not tested | TP53 (p.R273C), TMPRSS2-ERG fusion, AR amplification |
3 | 1 | MSH2 | Biallelic mutation in MSH2 (exon 3–16 dletion, with associated LOH); positive for microsatellite instability; TP53 (p.R273C), hypermutation with TMB of 20 mutations/Mb |
5 | 1 | None | TMPRSS2-ERG rearrangement |
9 | 2 | Unknown | BRCA2 deletions in exons 3–11 with LOH; PTEN deletion (exons 6- 8); FOXA1 in- frame insertion (c.797ins24); TP53 (p.C2777Gfs*63); APC (p.G520X) with LOH; AR amplification |
11 | 2 | Not Tested | None |
13 | 2 | Not Tested | TMPRSS2-ERG rearrangement |