Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42780 | A02 | 35609068 | G | A | synonymous_variant | LOW | c.165G>A|p.Glu55Glu |
S213 |
2 | BAA02g42780 | A02 | 35610399 | G | A | missense_variant | MODERATE | c.854G>A|p.Gly285Asp |
S25 |
3 | BAA02g42780 | A02 | 35610890 | C | T | missense_variant | MODERATE | c.1081C>T|p.Pro361Ser |
S32 |
4 | BAA02g42780 | A02 | 35611124 | C | T | synonymous_variant | LOW | c.1315C>T|p.Leu439Leu |
S38 |
5 | BAA02g42780 | A02 | 35611303 | C | T | stop_gained | HIGH | c.1381C>T|p.Gln461* |
S135 |
6 | BAA02g42780 | A02 | 35611337 | C | T | missense_variant | MODERATE | c.1415C>T|p.Thr472Ile |
S159 S243 |
7 | BAA02g42780 | A02 | 35611916 | G | A | missense_variant | MODERATE | c.1852G>A|p.Glu618Lys |
S34 |
8 | BAA02g42780 | A02 | 35612141 | G | A | missense_variant | MODERATE | c.2077G>A|p.Val693Ile |
S177 |
9 | BAA02g42780 | A02 | 35612280 | C | T | synonymous_variant | LOW | c.2131C>T|p.Leu711Leu |
S302 |
10 | BAA02g42780 | A02 | 35612561 | C | T | synonymous_variant | LOW | c.2338C>T|p.Leu780Leu |
S185 |
11 | BAA02g42780 | A02 | 35612748 | G | A | missense_variant | MODERATE | c.2374G>A|p.Glu792Lys |
S235 |