Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42140 | A02 | 35126076 | C | T | missense_variant | MODERATE | c.1717G>A|p.Ala573Thr |
S283 |
2 | BAA02g42140 | A02 | 35126115 | G | A | stop_gained | HIGH | c.1678C>T|p.Gln560* |
S223 |
3 | BAA02g42140 | A02 | 35126693 | G | A | missense_variant | MODERATE | c.1187C>T|p.Ala396Val |
S126 |
4 | BAA02g42140 | A02 | 35129549 | C | T | missense_variant | MODERATE | c.211G>A|p.Glu71Lys |
S42 |
5 | BAA02g42140 | A02 | 35130961 | G | A | upstream_gene_variant | MODIFIER | c.-1202C>T| |
S210 |
6 | BAA02g42140 | A02 | 35131055 | G | A | upstream_gene_variant | MODIFIER | c.-1296C>T| |
S265 |
7 | BAA02g42140 | A02 | 35131181 | C | T | upstream_gene_variant | MODIFIER | c.-1422G>A| |
S133 |
8 | BAA02g42140 | A02 | 35132863 | G | A | upstream_gene_variant | MODIFIER | c.-3104C>T| |
S259 |
9 | BAA02g42140 | A02 | 35133508 | G | A | upstream_gene_variant | MODIFIER | c.-3749C>T| |
S288 |