Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46400 | A02 | 37715080 | G | A | upstream_gene_variant | MODIFIER | c.-4402G>A| |
S288 |
2 | BAA02g46400 | A02 | 37715535 | C | T | upstream_gene_variant | MODIFIER | c.-3947C>T| |
S133 S268 |
3 | BAA02g46400 | A02 | 37715703 | G | A | upstream_gene_variant | MODIFIER | c.-3779G>A| |
S38 |
4 | BAA02g46400 | A02 | 37716605 | C | T | upstream_gene_variant | MODIFIER | c.-2877C>T| |
S270 |
5 | BAA02g46400 | A02 | 37716631 | G | A | upstream_gene_variant | MODIFIER | c.-2851G>A| |
S265 |
6 | BAA02g46400 | A02 | 37717940 | C | T | upstream_gene_variant | MODIFIER | c.-1542C>T| |
S51 |
7 | BAA02g46400 | A02 | 37719846 | C | T | missense_variant | MODERATE | c.365C>T|p.Ala122Val |
S85 |
8 | BAA02g46400 | A02 | 37720979 | G | A | synonymous_variant | LOW | c.546G>A|p.Val182Val |
S297 |