Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21000 | A02 | 11225141 | C | T | missense_variant | MODERATE | c.803G>A|p.Gly268Glu |
S112 |
2 | BAA02g21000 | A02 | 11225995 | G | A | missense_variant | MODERATE | c.194C>T|p.Thr65Ile |
S206 S26 |
3 | BAA02g21000 | A02 | 11226170 | C | T | missense_variant | MODERATE | c.19G>A|p.Ala7Thr |
S226 |
4 | BAA02g21000 | A02 | 11226231 | C | T | upstream_gene_variant | MODIFIER | c.-43G>A| |
S221 |
5 | BAA02g21000 | A02 | 11228652 | C | T | upstream_gene_variant | MODIFIER | c.-2464G>A| |
S270 |
6 | BAA02g21000 | A02 | 11228937 | C | T | upstream_gene_variant | MODIFIER | c.-2749G>A| |
S219 S72 |
7 | BAA02g21000 | A02 | 11229419 | G | A | upstream_gene_variant | MODIFIER | c.-3231C>T| |
S12 |
8 | BAA02g21000 | A02 | 11229463 | C | T | upstream_gene_variant | MODIFIER | c.-3275G>A| |
S249 |
9 | BAA02g21000 | A02 | 11229549 | G | A | upstream_gene_variant | MODIFIER | c.-3361C>T| |
S132 S215 |
10 | BAA02g21000 | A02 | 11231118 | G | A | upstream_gene_variant | MODIFIER | c.-4930C>T| |
S170 |