Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47840 | A02 | 38525454 | C | T | synonymous_variant | LOW | c.1017G>A|p.Gln339Gln |
S133 |
2 | BAA02g47840 | A02 | 38525531 | C | T | missense_variant | MODERATE | c.940G>A|p.Ala314Thr |
S264 |
3 | BAA02g47840 | A02 | 38525549 | C | T | missense_variant | MODERATE | c.922G>A|p.Gly308Arg |
S165 |
4 | BAA02g47840 | A02 | 38526696 | G | A | synonymous_variant | LOW | c.75C>T|p.Val25Val |
S5 |
5 | BAA02g47840 | A02 | 38528019 | C | T | upstream_gene_variant | MODIFIER | c.-1134G>A| |
S48 |
6 | BAA02g47840 | A02 | 38528834 | C | T | upstream_gene_variant | MODIFIER | c.-1949G>A| |
S117 |
7 | BAA02g47840 | A02 | 38528936 | G | A | upstream_gene_variant | MODIFIER | c.-2051C>T| |
S247 |
8 | BAA02g47840 | A02 | 38530001 | C | T | upstream_gene_variant | MODIFIER | c.-3116G>A| |
S249 |
9 | BAA02g47840 | A02 | 38531111 | G | A | upstream_gene_variant | MODIFIER | c.-4226C>T| |
S166 S167 S262 |
10 | BAA02g47840 | A02 | 38531711 | G | A | upstream_gene_variant | MODIFIER | c.-4826C>T| |
S11 |