Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00580 | A02 | 312246 | C | T | upstream_gene_variant | MODIFIER | c.-4573C>T| |
S216 |
2 | BAA02g00580 | A02 | 312291 | C | T | upstream_gene_variant | MODIFIER | c.-4528C>T| |
S207 |
3 | BAA02g00580 | A02 | 312630 | G | A | upstream_gene_variant | MODIFIER | c.-4189G>A| |
S128 |
4 | BAA02g00580 | A02 | 312866 | G | A | upstream_gene_variant | MODIFIER | c.-3953G>A| |
S64 |
5 | BAA02g00580 | A02 | 316917 | G | A | synonymous_variant | LOW | c.99G>A|p.Gln33Gln |
S295 |
6 | BAA02g00580 | A02 | 317507 | C | T | synonymous_variant | LOW | c.375C>T|p.Leu125Leu |
S85 |
7 | BAA02g00580 | A02 | 317578 | C | T | missense_variant | MODERATE | c.446C>T|p.Pro149Leu |
S251 |
8 | BAA02g00580 | A02 | 318118 | G | A | missense_variant | MODERATE | c.614G>A|p.Arg205Lys |
S4 |
9 | BAA02g00580 | A02 | 318656 | C | T | missense_variant | MODERATE | c.829C>T|p.Pro277Ser |
S201 |
10 | BAA02g00580 | A02 | 318671 | G | A | missense_variant | MODERATE | c.844G>A|p.Gly282Arg |
S87 |
11 | BAA02g00580 | A02 | 319739 | G | A | downstream_gene_variant | MODIFIER | c.*913G>A| |
S188 |
12 | BAA02g00580 | A02 | 319764 | C | T | downstream_gene_variant | MODIFIER | c.*938C>T| |
S228 |