Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03380 | A02 | 1494563 | G | A | missense_variant | MODERATE | c.374C>T|p.Thr125Ile |
S268 |
2 | BAA02g03380 | A02 | 1495139 | G | A | upstream_gene_variant | MODIFIER | c.-203C>T| |
S192 |
3 | BAA02g03380 | A02 | 1495664 | G | A | upstream_gene_variant | MODIFIER | c.-728C>T| |
S187 S298 |
4 | BAA02g03380 | A02 | 1497082 | G | A | upstream_gene_variant | MODIFIER | c.-2146C>T| |
S163 |
5 | BAA02g03380 | A02 | 1497307 | G | A | upstream_gene_variant | MODIFIER | c.-2371C>T| |
S283 |
6 | BAA02g03380 | A02 | 1498403 | G | A | upstream_gene_variant | MODIFIER | c.-3467C>T| |
S136 |
7 | BAA02g03380 | A02 | 1498613 | G | A | upstream_gene_variant | MODIFIER | c.-3677C>T| |
S244 |
8 | BAA02g03380 | A02 | 1499301 | C | T | upstream_gene_variant | MODIFIER | c.-4365G>A| |
S201 |