Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10110 | A02 | 4470709 | G | A | downstream_gene_variant | MODIFIER | c.*1385C>T| |
S247 |
2 | BAA02g10110 | A02 | 4472563 | G | A | missense_variant | MODERATE | c.281C>T|p.Thr94Met |
S125 |
3 | BAA02g10110 | A02 | 4473135 | G | A | upstream_gene_variant | MODIFIER | c.-206C>T| |
S170 |
4 | BAA02g10110 | A02 | 4473276 | C | T | upstream_gene_variant | MODIFIER | c.-347G>A| |
S32 |
5 | BAA02g10110 | A02 | 4473393 | T | G | upstream_gene_variant | MODIFIER | c.-464A>C| |
S272 |
6 | BAA02g10110 | A02 | 4473887 | G | A | upstream_gene_variant | MODIFIER | c.-958C>T| |
S283 |
7 | BAA02g10110 | A02 | 4475310 | G | A | upstream_gene_variant | MODIFIER | c.-2381C>T| |
S176 |
8 | BAA02g10110 | A02 | 4476242 | C | T | upstream_gene_variant | MODIFIER | c.-3313G>A| |
S207 |
9 | BAA02g10110 | A02 | 4476249 | G | A | upstream_gene_variant | MODIFIER | c.-3320C>T| |
S74 |
10 | BAA02g10110 | A02 | 4476780 | G | A | upstream_gene_variant | MODIFIER | c.-3851C>T| |
S23 |
11 | BAA02g10110 | A02 | 4476962 | G | A | upstream_gene_variant | MODIFIER | c.-4033C>T| |
S184 |
12 | BAA02g10110 | A02 | 4476970 | G | A | upstream_gene_variant | MODIFIER | c.-4041C>T| |
S163 |
13 | BAA02g10110 | A02 | 4477001 | G | A | upstream_gene_variant | MODIFIER | c.-4072C>T| |
S280 |