| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g33030 | A02 | 28293760 | C | T | downstream_gene_variant | MODIFIER | c.*4634G>A| |
S157 S163 |
| 2 | BAA02g33030 | A02 | 28294662 | C | T | downstream_gene_variant | MODIFIER | c.*3732G>A| |
S305 |
| 3 | BAA02g33030 | A02 | 28294981 | C | T | downstream_gene_variant | MODIFIER | c.*3413G>A| |
S94 |
| 4 | BAA02g33030 | A02 | 28297335 | C | T | downstream_gene_variant | MODIFIER | c.*1059G>A| |
S261 |
| 5 | BAA02g33030 | A02 | 28297390 | G | A | downstream_gene_variant | MODIFIER | c.*1004C>T| |
S174 |
| 6 | BAA02g33030 | A02 | 28297796 | C | T | downstream_gene_variant | MODIFIER | c.*598G>A| |
S65 |
| 7 | BAA02g33030 | A02 | 28298483 | C | T | missense_variant | MODERATE | c.709G>A|p.Gly237Ser |
S277 |
| 8 | BAA02g33030 | A02 | 28299007 | G | A | missense_variant | MODERATE | c.358C>T|p.Pro120Ser |
S47 |
| 9 | BAA02g33030 | A02 | 28299274 | C | T | missense_variant | MODERATE | c.208G>A|p.Val70Ile |
S273 |
| 10 | BAA02g33030 | A02 | 28300806 | G | A | upstream_gene_variant | MODIFIER | c.-1216C>T| |
S150 |
| 11 | BAA02g33030 | A02 | 28301310 | C | T | upstream_gene_variant | MODIFIER | c.-1720G>A| |
S284 |
| 12 | BAA02g33030 | A02 | 28301486 | G | A | upstream_gene_variant | MODIFIER | c.-1896C>T| |
S269 |
| 13 | BAA02g33030 | A02 | 28301678 | G | A | upstream_gene_variant | MODIFIER | c.-2088C>T| |
S297 |
| 14 | BAA02g33030 | A02 | 28301819 | G | A | upstream_gene_variant | MODIFIER | c.-2229C>T| |
S238 |
| 15 | BAA02g33030 | A02 | 28301884 | G | A | upstream_gene_variant | MODIFIER | c.-2294C>T| |
S98 |
| 16 | BAA02g33030 | A02 | 28302081 | T | C | upstream_gene_variant | MODIFIER | c.-2491A>G| |
S282 |
| 17 | BAA02g33030 | A02 | 28302546 | G | A | upstream_gene_variant | MODIFIER | c.-2956C>T| |
S268 |
| 18 | BAA02g33030 | A02 | 28302693 | G | A | upstream_gene_variant | MODIFIER | c.-3103C>T| |
S256 |