Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25230 | A02 | 13779134 | C | T | downstream_gene_variant | MODIFIER | c.*1425G>A| |
S168 S219 S278 S72 |
2 | BAA02g25230 | A02 | 13779741 | C | T | downstream_gene_variant | MODIFIER | c.*818G>A| |
S250 |
3 | BAA02g25230 | A02 | 13780636 | G | A | missense_variant | MODERATE | c.1549C>T|p.Leu517Phe |
S187 |
4 | BAA02g25230 | A02 | 13780846 | G | A | synonymous_variant | LOW | c.1407C>T|p.Thr469Thr |
S203 |
5 | BAA02g25230 | A02 | 13781044 | G | A | missense_variant | MODERATE | c.1279C>T|p.Pro427Ser |
S190 |
6 | BAA02g25230 | A02 | 13784380 | C | T | missense_variant | MODERATE | c.487G>A|p.Val163Ile |
S267 |
7 | BAA02g25230 | A02 | 13785092 | C | T | intron_variant | MODIFIER | c.252-477G>A| |
S165 |
8 | BAA02g25230 | A02 | 13786408 | C | T | upstream_gene_variant | MODIFIER | c.-298G>A| |
S246 |
9 | BAA02g25230 | A02 | 13786553 | G | A | upstream_gene_variant | MODIFIER | c.-443C>T| |
S259 |
10 | BAA02g25230 | A02 | 13787429 | C | T | upstream_gene_variant | MODIFIER | c.-1319G>A| |
S296 |
11 | BAA02g25230 | A02 | 13787775 | G | A | upstream_gene_variant | MODIFIER | c.-1665C>T| |
S288 |
12 | BAA02g25230 | A02 | 13787974 | C | T | upstream_gene_variant | MODIFIER | c.-1864G>A| |
S226 |
13 | BAA02g25230 | A02 | 13787983 | G | A | upstream_gene_variant | MODIFIER | c.-1873C>T| |
S81 S85 |
14 | BAA02g25230 | A02 | 13788317 | C | T | upstream_gene_variant | MODIFIER | c.-2207G>A| |
S97 |
15 | BAA02g25230 | A02 | 13790581 | C | T | upstream_gene_variant | MODIFIER | c.-4471G>A| |
S280 |
16 | BAA02g25230 | A02 | 13790688 | G | A | upstream_gene_variant | MODIFIER | c.-4578C>T| |
S158 |