Somatic mutations discovered by targeted SOLiD sequencing
| Gene | Base change | AA change | Percentage of sequencing reads | SIFT | Polyphen |
| % | |||||
| ATM | c.3616T>G | p.L1206V | 10 | Tolerated | Benign |
| ATM | c.3646T>C | p.Y1216H | 12 | Tolerated | Damaging (probably) |
| BRCA2 | c.2546T>C | p.V849A | 33 | Tolerated | Benign |
| BRCA2 | c.9966G>T | p.M3322I | 36 | Tolerated | Damaging (probably) |
| CHEK2 | c.1007A>T | p.Q336L | 54 | Damaging | Benign |
| DCLRE1C | c.1628_1632delTAACA | p.(I543Rfs*12) | 10 | - | - |
| DDB1 | c.26C>G | p.A9G | 86 | Damaging | Damaging (possibly) |
| EXO1 | c.1412A>G | p.K471R | 18 | Tolerated | Benign |
| MSH2 | c.1618A>G | p.S540G | 20 | Tolerated | Benign |
| MSH2 | c.2497C>G | p.L833V | 50 | Damaging | Benign |
| MSH6 | c.1628A>G | p.K543R | 29 | Damaging | Benign |
| PARP1 | c.1910_1922delinsGTT | p.(K637Sfs*13) | 18 | - | - |
| PRKDC | c.10252T>C | p.F3418L | 31 | Damaging | Damaging (probably) |
| TNFAIP3 | c.1877_1878delTG | p.(C627Ffs*44) | 20 | - | - |
| TP53 | c.400T>G | p.F134V | 47 | Damaging | Damaging (probably) |
| TP53 | c.817C>T | p.R273C | 67 | Damaging | Damaging (probably) |
| TP53 | c.818G>A | p.R273H | 38 | Damaging | Damaging (probably) |
| XRCC5 | c.847A>G | p.T283A | 29 | Damaging | Damaging (probably) |
| XRCC6 | c.800delT | p.(I267Kfs*2) | 28 | - | - |
| Gene | Base change | AA change | Percentage of sequencing reads | SIFT | Polyphen |
| % | |||||
| ATM | c.3616T>G | p.L1206V | 10 | Tolerated | Benign |
| ATM | c.3646T>C | p.Y1216H | 12 | Tolerated | Damaging (probably) |
| BRCA2 | c.2546T>C | p.V849A | 33 | Tolerated | Benign |
| BRCA2 | c.9966G>T | p.M3322I | 36 | Tolerated | Damaging (probably) |
| CHEK2 | c.1007A>T | p.Q336L | 54 | Damaging | Benign |
| DCLRE1C | c.1628_1632delTAACA | p.(I543Rfs*12) | 10 | - | - |
| DDB1 | c.26C>G | p.A9G | 86 | Damaging | Damaging (possibly) |
| EXO1 | c.1412A>G | p.K471R | 18 | Tolerated | Benign |
| MSH2 | c.1618A>G | p.S540G | 20 | Tolerated | Benign |
| MSH2 | c.2497C>G | p.L833V | 50 | Damaging | Benign |
| MSH6 | c.1628A>G | p.K543R | 29 | Damaging | Benign |
| PARP1 | c.1910_1922delinsGTT | p.(K637Sfs*13) | 18 | - | - |
| PRKDC | c.10252T>C | p.F3418L | 31 | Damaging | Damaging (probably) |
| TNFAIP3 | c.1877_1878delTG | p.(C627Ffs*44) | 20 | - | - |
| TP53 | c.400T>G | p.F134V | 47 | Damaging | Damaging (probably) |
| TP53 | c.817C>T | p.R273C | 67 | Damaging | Damaging (probably) |
| TP53 | c.818G>A | p.R273H | 38 | Damaging | Damaging (probably) |
| XRCC5 | c.847A>G | p.T283A | 29 | Damaging | Damaging (probably) |
| XRCC6 | c.800delT | p.(I267Kfs*2) | 28 | - | - |