Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34900 | A02 | 30037469 | G | A | upstream_gene_variant | MODIFIER | c.-321G>A| |
S256 |
2 | BAA02g34900 | A02 | 30038516 | C | T | synonymous_variant | LOW | c.465C>T|p.Val155Val |
S100 |
3 | BAA02g34900 | A02 | 30039187 | C | T | missense_variant | MODERATE | c.856C>T|p.Pro286Ser |
S255 |
4 | BAA02g34900 | A02 | 30039229 | C | T | intron_variant | MODIFIER | c.879+19C>T| |
S2 |
5 | BAA02g34900 | A02 | 30039984 | G | A | intron_variant | MODIFIER | c.981-82G>A| |
S265 |
6 | BAA02g34900 | A02 | 30040389 | G | A | intron_variant | MODIFIER | c.1138-53G>A| |
S279 |
7 | BAA02g34900 | A02 | 30041225 | C | T | downstream_gene_variant | MODIFIER | c.*691C>T| |
S130 |
8 | BAA02g34900 | A02 | 30042023 | C | T | downstream_gene_variant | MODIFIER | c.*1489C>T| |
S9 |
9 | BAA02g34900 | A02 | 30042261 | G | A | downstream_gene_variant | MODIFIER | c.*1727G>A| |
S197 |
10 | BAA02g34900 | A02 | 30042340 | C | T | downstream_gene_variant | MODIFIER | c.*1806C>T| |
S42 |
11 | BAA02g34900 | A02 | 30042626 | C | T | downstream_gene_variant | MODIFIER | c.*2092C>T| |
S37 |
12 | BAA02g34900 | A02 | 30042636 | G | A | downstream_gene_variant | MODIFIER | c.*2102G>A| |
S96 |
13 | BAA02g34900 | A02 | 30043831 | G | A | downstream_gene_variant | MODIFIER | c.*3297G>A| |
S217 S248 |
14 | BAA02g34900 | A02 | 30043930 | G | A | downstream_gene_variant | MODIFIER | c.*3396G>A| |
S169 |
15 | BAA02g34900 | A02 | 30044350 | G | A | downstream_gene_variant | MODIFIER | c.*3816G>A| |
S43 |
16 | BAA02g34900 | A02 | 30044760 | C | T | downstream_gene_variant | MODIFIER | c.*4226C>T| |
S277 |