Tumor area. | Chromosome | Position | Gene | Variant type | HGVS.c | Protein change | VAF |
---|---|---|---|---|---|---|---|
EBV-positive | Chr1 | 26,774,684 | ARID1A | Frameshift mutation | c.4458_4477delGGCATCAGCTGAGGTTGCTC | p.Ser1488fs | 0.059 |
EBV-positive | Chr17 | 70,175,263 | KCNJ2 | Missense mutation | c.224 C > T | p.Thr75Met | 0.083 |
EBV-positive | chr11 | 14,358,803 | RRAS2 | Missense mutation | c.68G > T | p.Gly23Val | 0.067 |
EBV-positive | chr15 | 44,715,574 | B2M | Frameshift mutation | c.220_233delTTGTCTTTCAGCAA | p.Leu74fs | 0.012 |
EBV-positive | Chr6 | 29,944,149 | HLA-A | Frameshift mutation | c.650_651dupCC | p.Ile218fs | 0.027 |
EBV-positive | chrX | 45,089,874 | KDM6A | Nonsense mutation | c.3836G > A | p.Trp1279* | 0.139 |
EBV-negative | Chr1 | 26,774,684 | ARID1A | Frameshift mutation | c.4458_4477delGGCATCAGCTGAGGTTGCTC | p.Ser1488fs | 0.126 |
EBV-negative | Chr17 | 70,175,263 | KCNJ2 | Missense mutation | c.224 C > T | p.Thr75Met | 0.203 |
EBV-negative | chr11 | 14,358,803 | RRAS2 | Missense mutation | c.68G > T | p.Gly23Val | 0.175 |
EBV-negative | Chr3 | 179,218,294 | PIK3CA | Missense mutation | c.1624G > A | p.Glu542Lys | 0.078 |
EBV-negative | chr17 | 7,673,803 | TP53 | Missense mutation | c.817 C > T | p.Arg273Cys | 0.272 |