Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20080 | A02 | 10577191 | G | A | downstream_gene_variant | MODIFIER | c.*4696C>T| |
S257 |
2 | BAA02g20080 | A02 | 10582783 | G | A | splice_region_variant&intron_variant | LOW | c.655-6C>T| |
S197 |
3 | BAA02g20080 | A02 | 10582931 | C | T | synonymous_variant | LOW | c.585G>A|p.Leu195Leu |
S301 S304 |
4 | BAA02g20080 | A02 | 10583069 | G | A | synonymous_variant | LOW | c.447C>T|p.Leu149Leu |
S282 |
5 | BAA02g20080 | A02 | 10583073 | G | A | missense_variant | MODERATE | c.443C>T|p.Ser148Phe |
S28 |
6 | BAA02g20080 | A02 | 10583152 | G | A | intron_variant | MODIFIER | c.388-24C>T| |
S107 |
7 | BAA02g20080 | A02 | 10584055 | C | T | intron_variant | MODIFIER | c.388-927G>A| |
S40 S49 |
8 | BAA02g20080 | A02 | 10584382 | C | T | intron_variant | MODIFIER | c.388-1254G>A| |
S163 S183 S198 |
9 | BAA02g20080 | A02 | 10584407 | C | G | intron_variant | MODIFIER | c.388-1279G>C| |
S109 |
10 | BAA02g20080 | A02 | 10584459 | C | T | intron_variant | MODIFIER | c.388-1331G>A| |
S51 |
11 | BAA02g20080 | A02 | 10586416 | C | T | intron_variant | MODIFIER | c.387+1016G>A| |
S270 |
12 | BAA02g20080 | A02 | 10587833 | C | T | intron_variant | MODIFIER | c.100-114G>A| |
S82 S92 |