Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04060 | A02 | 1763411 | A | G | downstream_gene_variant | MODIFIER | c.*1635T>C| |
S299 |
2 | BAA02g04060 | A02 | 1764812 | C | T | downstream_gene_variant | MODIFIER | c.*234G>A| |
S288 |
3 | BAA02g04060 | A02 | 1764950 | G | A | downstream_gene_variant | MODIFIER | c.*96C>T| |
S107 |
4 | BAA02g04060 | A02 | 1765195 | G | A | stop_gained | HIGH | c.1402C>T|p.Gln468* |
S256 |
5 | BAA02g04060 | A02 | 1767636 | G | T | missense_variant | MODERATE | c.1049C>A|p.Pro350His |
S178 |
6 | BAA02g04060 | A02 | 1768248 | C | T | missense_variant | MODERATE | c.437G>A|p.Gly146Glu |
S211 S227 |
7 | BAA02g04060 | A02 | 1768399 | C | T | missense_variant | MODERATE | c.286G>A|p.Glu96Lys |
S306 |
8 | BAA02g04060 | A02 | 1768770 | G | A | upstream_gene_variant | MODIFIER | c.-86C>T| |
S244 |
9 | BAA02g04060 | A02 | 1769950 | G | A | upstream_gene_variant | MODIFIER | c.-1266C>T| |
S126 |
10 | BAA02g04060 | A02 | 1770186 | T | C | upstream_gene_variant | MODIFIER | c.-1502A>G| |
S181 S217 S248 |
11 | BAA02g04060 | A02 | 1770271 | G | A | upstream_gene_variant | MODIFIER | c.-1587C>T| |
S261 S303 |
12 | BAA02g04060 | A02 | 1771303 | C | T | upstream_gene_variant | MODIFIER | c.-2619G>A| |
S182 |
13 | BAA02g04060 | A02 | 1772226 | C | T | upstream_gene_variant | MODIFIER | c.-3542G>A| |
S34 |
14 | BAA02g04060 | A02 | 1772228 | C | T | upstream_gene_variant | MODIFIER | c.-3544G>A| |
S150 |
15 | BAA02g04060 | A02 | 1772648 | C | T | upstream_gene_variant | MODIFIER | c.-3964G>A| |
S219 S72 |
16 | BAA02g04060 | A02 | 1772865 | G | A | upstream_gene_variant | MODIFIER | c.-4181C>T| |
S153 S213 |