| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g07770 | A02 | 3340569 | G | A | downstream_gene_variant | MODIFIER | c.*4237C>T| |
S158 |
| 2 | BAA02g07770 | A02 | 3341192 | G | A | downstream_gene_variant | MODIFIER | c.*3614C>T| |
S105 S106 |
| 3 | BAA02g07770 | A02 | 3344988 | C | T | missense_variant | MODERATE | c.661G>A|p.Val221Ile |
S295 |
| 4 | BAA02g07770 | A02 | 3345790 | G | A | missense_variant | MODERATE | c.128C>T|p.Ser43Phe |
S161 |
| 5 | BAA02g07770 | A02 | 3346719 | C | T | upstream_gene_variant | MODIFIER | c.-802G>A| |
S81 |
| 6 | BAA02g07770 | A02 | 3346866 | C | T | upstream_gene_variant | MODIFIER | c.-949G>A| |
S229 |
| 7 | BAA02g07770 | A02 | 3347589 | C | T | upstream_gene_variant | MODIFIER | c.-1672G>A| |
S233 |
| 8 | BAA02g07770 | A02 | 3347909 | C | T | upstream_gene_variant | MODIFIER | c.-1992G>A| |
S116 S229 |
| 9 | BAA02g07770 | A02 | 3349021 | C | T | upstream_gene_variant | MODIFIER | c.-3104G>A| |
S8 |
| 10 | BAA02g07770 | A02 | 3349120 | G | A | upstream_gene_variant | MODIFIER | c.-3203C>T| |
S163 |
| 11 | BAA02g07770 | A02 | 3349202 | G | A | upstream_gene_variant | MODIFIER | c.-3285C>T| |
S127 |
| 12 | BAA02g07770 | A02 | 3349346 | C | T | upstream_gene_variant | MODIFIER | c.-3429G>A| |
S287 |
| 13 | BAA02g07770 | A02 | 3349930 | C | T | upstream_gene_variant | MODIFIER | c.-4013G>A| |
S9 |
| 14 | BAA02g07770 | A02 | 3350678 | C | T | upstream_gene_variant | MODIFIER | c.-4761G>A| |
S216 |
| 15 | BAA02g07770 | A02 | 3350782 | C | T | upstream_gene_variant | MODIFIER | c.-4865G>A| |
S245 |