Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15900 | A02 | 7741231 | C | T | downstream_gene_variant | MODIFIER | c.*2078G>A| |
S142 |
2 | BAA02g15900 | A02 | 7741262 | C | A | downstream_gene_variant | MODIFIER | c.*2047G>T| |
S57 |
3 | BAA02g15900 | A02 | 7743422 | C | T | missense_variant | MODERATE | c.1012G>A|p.Ala338Thr |
S55 |
4 | BAA02g15900 | A02 | 7745178 | C | A | missense_variant | MODERATE | c.202G>T|p.Gly68Cys |
S44 |
5 | BAA02g15900 | A02 | 7745226 | G | A | missense_variant | MODERATE | c.154C>T|p.Pro52Ser |
S64 |
6 | BAA02g15900 | A02 | 7748250 | G | A | upstream_gene_variant | MODIFIER | c.-2871C>T| |
S43 |
7 | BAA02g15900 | A02 | 7748465 | G | A | upstream_gene_variant | MODIFIER | c.-3086C>T| |
S192 |
8 | BAA02g15900 | A02 | 7749018 | G | A | upstream_gene_variant | MODIFIER | c.-3639C>T| |
S35 |
9 | BAA02g15900 | A02 | 7749059 | G | A | upstream_gene_variant | MODIFIER | c.-3680C>T| |
S100 |
10 | BAA02g15900 | A02 | 7749400 | G | A | upstream_gene_variant | MODIFIER | c.-4021C>T| |
S45 |