Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04860 | A02 | 2116645 | C | T | downstream_gene_variant | MODIFIER | c.*996G>A| |
S212 |
2 | BAA02g04860 | A02 | 2118371 | C | T | missense_variant | MODERATE | c.677G>A|p.Arg226Gln |
S200 |
3 | BAA02g04860 | A02 | 2118479 | G | A | missense_variant | MODERATE | c.569C>T|p.Ala190Val |
S67 |
4 | BAA02g04860 | A02 | 2119449 | G | A | missense_variant | MODERATE | c.115C>T|p.Leu39Phe |
S305 |
5 | BAA02g04860 | A02 | 2119469 | G | A | missense_variant | MODERATE | c.95C>T|p.Ser32Leu |
S82 S92 |
6 | BAA02g04860 | A02 | 2121177 | G | A | upstream_gene_variant | MODIFIER | c.-1614C>T| |
S239 |
7 | BAA02g04860 | A02 | 2121203 | C | T | upstream_gene_variant | MODIFIER | c.-1640G>A| |
S262 |
8 | BAA02g04860 | A02 | 2121215 | C | T | upstream_gene_variant | MODIFIER | c.-1652G>A| |
S250 |
9 | BAA02g04860 | A02 | 2123838 | C | T | upstream_gene_variant | MODIFIER | c.-4275G>A| |
S251 |
10 | BAA02g04860 | A02 | 2124426 | C | T | upstream_gene_variant | MODIFIER | c.-4863G>A| |
S229 |
11 | BAA02g04860 | A02 | 2124525 | G | A | upstream_gene_variant | MODIFIER | c.-4962C>T| |
S192 |