Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35770 | A02 | 30822469 | G | A | upstream_gene_variant | MODIFIER | c.-2642G>A| |
S94 |
2 | BAA02g35770 | A02 | 30824326 | G | A | upstream_gene_variant | MODIFIER | c.-785G>A| |
S286 |
3 | BAA02g35770 | A02 | 30824386 | G | A | upstream_gene_variant | MODIFIER | c.-725G>A| |
S260 |
4 | BAA02g35770 | A02 | 30825129 | C | T | synonymous_variant | LOW | c.19C>T|p.Leu7Leu |
S277 |
5 | BAA02g35770 | A02 | 30825220 | G | A | missense_variant | MODERATE | c.110G>A|p.Gly37Glu |
S229 |
6 | BAA02g35770 | A02 | 30825465 | C | T | missense_variant | MODERATE | c.278C>T|p.Ser93Phe |
S88 |
7 | BAA02g35770 | A02 | 30826363 | C | T | synonymous_variant | LOW | c.615C>T|p.Ile205Ile |
S33 |
8 | BAA02g35770 | A02 | 30826630 | G | A | intron_variant | MODIFIER | c.635-37G>A| |
S136 |
9 | BAA02g35770 | A02 | 30827112 | G | A | missense_variant | MODERATE | c.829G>A|p.Gly277Ser |
S143 |
10 | BAA02g35770 | A02 | 30827136 | G | A | missense_variant | MODERATE | c.853G>A|p.Gly285Arg |
S225 S73 |
11 | BAA02g35770 | A02 | 30828513 | G | A | synonymous_variant | LOW | c.1323G>A|p.Arg441Arg |
S251 |
12 | BAA02g35770 | A02 | 30828522 | C | T | synonymous_variant | LOW | c.1332C>T|p.Val444Val |
S299 |
13 | BAA02g35770 | A02 | 30829582 | G | A | downstream_gene_variant | MODIFIER | c.*814G>A| |
S158 |