| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g21720 | A05 | 20814109 | C | T | upstream_gene_variant | MODIFIER | c.-114C>T| |
S297 |
| 2 | BAA05g21720 | A05 | 20814147 | C | T | upstream_gene_variant | MODIFIER | c.-76C>T| |
S73 S91 |
| 3 | BAA05g21720 | A05 | 20814766 | C | T | missense_variant | MODERATE | c.544C>T|p.Pro182Ser |
S206 S26 |
| 4 | BAA05g21720 | A05 | 20814925 | C | T | missense_variant | MODERATE | c.703C>T|p.Leu235Phe |
S195 |
| 5 | BAA05g21720 | A05 | 20815004 | C | T | missense_variant | MODERATE | c.782C>T|p.Ala261Val |
S273 S33 |
| 6 | BAA05g21720 | A05 | 20815031 | C | T | intron_variant | MODIFIER | c.798+11C>T| |
S306 S308 |
| 7 | BAA05g21720 | A05 | 20815190 | G | A | synonymous_variant | LOW | c.882G>A|p.Arg294Arg |
S200 |
| 8 | BAA05g21720 | A05 | 20816037 | G | A | downstream_gene_variant | MODIFIER | c.*634G>A| |
S134 |
| 9 | BAA05g21720 | A05 | 20816062 | G | A | downstream_gene_variant | MODIFIER | c.*659G>A| |
S136 |
| 10 | BAA05g21720 | A05 | 20816398 | G | A | downstream_gene_variant | MODIFIER | c.*995G>A| |
S196 |
| 11 | BAA05g21720 | A05 | 20816664 | G | A | downstream_gene_variant | MODIFIER | c.*1261G>A| |
S40 S49 |