Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g27980 | A03 | 12946758 | G | A | upstream_gene_variant | MODIFIER | c.-4025G>A| |
S200 |
2 | BAA03g27980 | A03 | 12946850 | G | A | upstream_gene_variant | MODIFIER | c.-3933G>A| |
S206 S26 |
3 | BAA03g27980 | A03 | 12948146 | C | T | upstream_gene_variant | MODIFIER | c.-2637C>T| |
S156 |
4 | BAA03g27980 | A03 | 12948241 | C | T | upstream_gene_variant | MODIFIER | c.-2542C>T| |
S225 S73 |
5 | BAA03g27980 | A03 | 12948250 | C | T | upstream_gene_variant | MODIFIER | c.-2533C>T| |
S170 |
6 | BAA03g27980 | A03 | 12948335 | C | T | upstream_gene_variant | MODIFIER | c.-2448C>T| |
S244 |
7 | BAA03g27980 | A03 | 12948404 | G | A | upstream_gene_variant | MODIFIER | c.-2379G>A| |
S78 |
8 | BAA03g27980 | A03 | 12949840 | C | T | upstream_gene_variant | MODIFIER | c.-943C>T| |
S301 |
9 | BAA03g27980 | A03 | 12951656 | G | A | missense_variant | MODERATE | c.874G>A|p.Ala292Thr |
S288 |