| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g12100 | A01 | 5659704 | G | A | downstream_gene_variant | MODIFIER | c.*2276C>T| |
S37 |
| 2 | BAA01g12100 | A01 | 5661529 | C | T | downstream_gene_variant | MODIFIER | c.*451G>A| |
S291 |
| 3 | BAA01g12100 | A01 | 5661601 | G | A | downstream_gene_variant | MODIFIER | c.*379C>T| |
S235 |
| 4 | BAA01g12100 | A01 | 5661854 | G | A | downstream_gene_variant | MODIFIER | c.*126C>T| |
S236 |
| 5 | BAA01g12100 | A01 | 5662179 | C | T | missense_variant | MODERATE | c.692G>A|p.Gly231Glu |
S226 |
| 6 | BAA01g12100 | A01 | 5662335 | C | T | missense_variant | MODERATE | c.536G>A|p.Arg179Gln |
S134 |
| 7 | BAA01g12100 | A01 | 5662367 | C | T | synonymous_variant | LOW | c.504G>A|p.Arg168Arg |
S286 |
| 8 | BAA01g12100 | A01 | 5662592 | C | T | synonymous_variant | LOW | c.279G>A|p.Leu93Leu |
S268 |
| 9 | BAA01g12100 | A01 | 5662738 | C | T | missense_variant | MODERATE | c.133G>A|p.Ala45Thr |
S1 S90 |
| 10 | BAA01g12100 | A01 | 5663993 | G | A | upstream_gene_variant | MODIFIER | c.-986C>T| |
S297 |
| 11 | BAA01g12100 | A01 | 5664475 | C | T | upstream_gene_variant | MODIFIER | c.-1468G>A| |
S202 |
| 12 | BAA01g12100 | A01 | 5664627 | C | T | upstream_gene_variant | MODIFIER | c.-1620G>A| |
S303 |
| 13 | BAA01g12100 | A01 | 5665454 | C | T | upstream_gene_variant | MODIFIER | c.-2447G>A| |
S278 |
| 14 | BAA01g12100 | A01 | 5665547 | A | T | upstream_gene_variant | MODIFIER | c.-2540T>A| |
S208 S219 |
| 15 | BAA01g12100 | A01 | 5666876 | G | A | upstream_gene_variant | MODIFIER | c.-3869C>T| |
S142 |
| 16 | BAA01g12100 | A01 | 5666968 | G | A | upstream_gene_variant | MODIFIER | c.-3961C>T| |
S278 |
| 17 | BAA01g12100 | A01 | 5667295 | C | T | upstream_gene_variant | MODIFIER | c.-4288G>A| |
S70 |
| 18 | BAA01g12100 | A01 | 5667314 | G | A | upstream_gene_variant | MODIFIER | c.-4307C>T| |
S240 |
| 19 | BAA01g12100 | A01 | 5667427 | G | A | upstream_gene_variant | MODIFIER | c.-4420C>T| |
S262 |