Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41880 | A02 | 34987289 | C | T | missense_variant | MODERATE | c.1132G>A|p.Val378Met |
S259 |
2 | BAA02g41880 | A02 | 34987393 | G | A | missense_variant | MODERATE | c.1028C>T|p.Ala343Val |
S23 |
3 | BAA02g41880 | A02 | 34988824 | C | T | missense_variant | MODERATE | c.194G>A|p.Gly65Glu |
S138 |
4 | BAA02g41880 | A02 | 34989832 | G | A | upstream_gene_variant | MODIFIER | c.-632C>T| |
S255 |
5 | BAA02g41880 | A02 | 34989861 | G | A | upstream_gene_variant | MODIFIER | c.-661C>T| |
S177 |
6 | BAA02g41880 | A02 | 34990879 | G | A | upstream_gene_variant | MODIFIER | c.-1679C>T| |
S159 S243 |
7 | BAA02g41880 | A02 | 34992628 | G | A | upstream_gene_variant | MODIFIER | c.-3428C>T| |
S183 |
8 | BAA02g41880 | A02 | 34993275 | C | T | upstream_gene_variant | MODIFIER | c.-4075G>A| |
S131 |
9 | BAA02g41880 | A02 | 34993742 | G | A | upstream_gene_variant | MODIFIER | c.-4542C>T| |
S19 |
10 | BAA02g41880 | A02 | 34993776 | C | T | upstream_gene_variant | MODIFIER | c.-4576G>A| |
S221 |
11 | BAA02g41880 | A02 | 34993896 | C | T | upstream_gene_variant | MODIFIER | c.-4696G>A| |
S255 |
12 | BAA02g41880 | A02 | 34994190 | C | T | upstream_gene_variant | MODIFIER | c.-4990G>A| |
S87 |