Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42070 | A02 | 35083383 | C | T | upstream_gene_variant | MODIFIER | c.-4996C>T| |
S108 |
2 | BAA02g42070 | A02 | 35084796 | A | T | upstream_gene_variant | MODIFIER | c.-3583A>T| |
S168 |
3 | BAA02g42070 | A02 | 35084868 | C | T | upstream_gene_variant | MODIFIER | c.-3511C>T| |
S59 |
4 | BAA02g42070 | A02 | 35085788 | G | A | upstream_gene_variant | MODIFIER | c.-2591G>A| |
S84 S93 |
5 | BAA02g42070 | A02 | 35086328 | C | T | upstream_gene_variant | MODIFIER | c.-2051C>T| |
S42 |
6 | BAA02g42070 | A02 | 35086440 | G | A | upstream_gene_variant | MODIFIER | c.-1939G>A| |
S18 |
7 | BAA02g42070 | A02 | 35086465 | C | T | upstream_gene_variant | MODIFIER | c.-1914C>T| |
S204 |
8 | BAA02g42070 | A02 | 35087394 | G | A | upstream_gene_variant | MODIFIER | c.-985G>A| |
S292 |
9 | BAA02g42070 | A02 | 35087398 | G | A | upstream_gene_variant | MODIFIER | c.-981G>A| |
S125 |
10 | BAA02g42070 | A02 | 35087531 | G | A | upstream_gene_variant | MODIFIER | c.-848G>A| |
S265 |
11 | BAA02g42070 | A02 | 35088650 | C | T | missense_variant | MODERATE | c.197C>T|p.Ser66Leu |
S116 |
12 | BAA02g42070 | A02 | 35090129 | C | T | intron_variant | MODIFIER | c.700-490C>T| |
S124 |
13 | BAA02g42070 | A02 | 35092500 | G | A | downstream_gene_variant | MODIFIER | c.*1053G>A| |
S287 |
14 | BAA02g42070 | A02 | 35093810 | C | T | downstream_gene_variant | MODIFIER | c.*2363C>T| |
S274 |