Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g20080 | A05 | 12229176 | C | T | upstream_gene_variant | MODIFIER | c.-4690C>T| |
S71 |
2 | BAA05g20080 | A05 | 12230166 | A | T | upstream_gene_variant | MODIFIER | c.-3700A>T| |
S186 |
3 | BAA05g20080 | A05 | 12230185 | C | T | upstream_gene_variant | MODIFIER | c.-3681C>T| |
S83 |
4 | BAA05g20080 | A05 | 12230207 | G | A | upstream_gene_variant | MODIFIER | c.-3659G>A| |
S257 |
5 | BAA05g20080 | A05 | 12230265 | C | T | upstream_gene_variant | MODIFIER | c.-3601C>T| |
S178 |
6 | BAA05g20080 | A05 | 12232387 | C | T | upstream_gene_variant | MODIFIER | c.-1479C>T| |
S267 |
7 | BAA05g20080 | A05 | 12233258 | G | A | upstream_gene_variant | MODIFIER | c.-608G>A| |
S129 |
8 | BAA05g20080 | A05 | 12233732 | G | A | upstream_gene_variant | MODIFIER | c.-134G>A| |
S266 |
9 | BAA05g20080 | A05 | 12234136 | G | A | stop_gained | HIGH | c.189G>A|p.Trp63* |
S94 |
10 | BAA05g20080 | A05 | 12235204 | C | T | missense_variant | MODERATE | c.601C>T|p.Pro201Ser |
S165 |
11 | BAA05g20080 | A05 | 12235312 | G | A | missense_variant | MODERATE | c.709G>A|p.Ala237Thr |
S46 |