Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16190 | A02 | 7893765 | G | A | downstream_gene_variant | MODIFIER | c.*2023C>T| |
S36 |
2 | BAA02g16190 | A02 | 7896015 | C | T | missense_variant | MODERATE | c.751G>A|p.Val251Met |
S112 |
3 | BAA02g16190 | A02 | 7896117 | C | T | missense_variant | MODERATE | c.649G>A|p.Gly217Ser |
S174 |
4 | BAA02g16190 | A02 | 7896164 | C | T | missense_variant | MODERATE | c.602G>A|p.Gly201Glu |
S174 |
5 | BAA02g16190 | A02 | 7896479 | G | A | missense_variant | MODERATE | c.287C>T|p.Ser96Phe |
S36 |
6 | BAA02g16190 | A02 | 7900278 | C | T | upstream_gene_variant | MODIFIER | c.-3513G>A| |
S240 |
7 | BAA02g16190 | A02 | 7900541 | G | A | upstream_gene_variant | MODIFIER | c.-3776C>T| |
S61 |
8 | BAA02g16190 | A02 | 7900723 | C | T | upstream_gene_variant | MODIFIER | c.-3958G>A| |
S283 |
9 | BAA02g16190 | A02 | 7901259 | G | A | upstream_gene_variant | MODIFIER | c.-4494C>T| |
S228 |
10 | BAA02g16190 | A02 | 7901265 | A | G | upstream_gene_variant | MODIFIER | c.-4500T>C| |
S200 |
11 | BAA02g16190 | A02 | 7901429 | C | T | upstream_gene_variant | MODIFIER | c.-4664G>A| |
S112 |