Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14780 | A02 | 6969118 | G | A | upstream_gene_variant | MODIFIER | c.-4158G>A| |
S202 |
2 | BAA02g14780 | A02 | 6969348 | C | T | upstream_gene_variant | MODIFIER | c.-3928C>T| |
S210 |
3 | BAA02g14780 | A02 | 6969717 | C | T | upstream_gene_variant | MODIFIER | c.-3559C>T| |
S44 |
4 | BAA02g14780 | A02 | 6969752 | C | T | upstream_gene_variant | MODIFIER | c.-3524C>T| |
S283 |
5 | BAA02g14780 | A02 | 6969840 | G | A | upstream_gene_variant | MODIFIER | c.-3436G>A| |
S223 |
6 | BAA02g14780 | A02 | 6970517 | C | T | upstream_gene_variant | MODIFIER | c.-2759C>T| |
S97 |
7 | BAA02g14780 | A02 | 6971140 | G | A | upstream_gene_variant | MODIFIER | c.-2136G>A| |
S23 |
8 | BAA02g14780 | A02 | 6972875 | C | T | upstream_gene_variant | MODIFIER | c.-401C>T| |
S179 |
9 | BAA02g14780 | A02 | 6973063 | G | A | upstream_gene_variant | MODIFIER | c.-213G>A| |
S28 |
10 | BAA02g14780 | A02 | 6973344 | C | T | synonymous_variant | LOW | c.69C>T|p.Pro23Pro |
S208 |
11 | BAA02g14780 | A02 | 6974142 | C | T | missense_variant | MODERATE | c.245C>T|p.Pro82Leu |
S199 |
12 | BAA02g14780 | A02 | 6974855 | G | A | missense_variant | MODERATE | c.716G>A|p.Arg239Lys |
S276 |
13 | BAA02g14780 | A02 | 6976507 | C | T | downstream_gene_variant | MODIFIER | c.*612C>T| |
S233 |
14 | BAA02g14780 | A02 | 6978012 | G | A | downstream_gene_variant | MODIFIER | c.*2117G>A| |
S198 |