| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g19740 | A01 | 9725721 | C | T | downstream_gene_variant | MODIFIER | c.*4954G>A| |
S123 S159 S243 |
| 2 | BAA01g19740 | A01 | 9725731 | G | A | downstream_gene_variant | MODIFIER | c.*4944C>T| |
S229 |
| 3 | BAA01g19740 | A01 | 9725825 | G | A | downstream_gene_variant | MODIFIER | c.*4850C>T| |
S208 S219 |
| 4 | BAA01g19740 | A01 | 9725947 | G | A | downstream_gene_variant | MODIFIER | c.*4728C>T| |
S28 |
| 5 | BAA01g19740 | A01 | 9730030 | G | A | downstream_gene_variant | MODIFIER | c.*645C>T| |
S195 |
| 6 | BAA01g19740 | A01 | 9730092 | G | A | downstream_gene_variant | MODIFIER | c.*583C>T| |
S162 |
| 7 | BAA01g19740 | A01 | 9730100 | G | A | downstream_gene_variant | MODIFIER | c.*575C>T| |
S239 |
| 8 | BAA01g19740 | A01 | 9730271 | G | A | downstream_gene_variant | MODIFIER | c.*404C>T| |
S67 |
| 9 | BAA01g19740 | A01 | 9730281 | C | T | downstream_gene_variant | MODIFIER | c.*394G>A| |
S128 |
| 10 | BAA01g19740 | A01 | 9731189 | C | T | upstream_gene_variant | MODIFIER | c.-101G>A| |
S41 |
| 11 | BAA01g19740 | A01 | 9731228 | G | A | upstream_gene_variant | MODIFIER | c.-140C>T| |
S291 |
| 12 | BAA01g19740 | A01 | 9731513 | G | A | upstream_gene_variant | MODIFIER | c.-425C>T| |
S58 |
| 13 | BAA01g19740 | A01 | 9731645 | G | A | upstream_gene_variant | MODIFIER | c.-557C>T| |
S43 |
| 14 | BAA01g19740 | A01 | 9732683 | G | A | upstream_gene_variant | MODIFIER | c.-1595C>T| |
S57 |
| 15 | BAA01g19740 | A01 | 9733692 | G | A | upstream_gene_variant | MODIFIER | c.-2604C>T| |
S71 |
| 16 | BAA01g19740 | A01 | 9735475 | C | T | upstream_gene_variant | MODIFIER | c.-4387G>A| |
S170 |
| 17 | BAA01g19740 | A01 | 9735570 | C | T | upstream_gene_variant | MODIFIER | c.-4482G>A| |
S79 |
| 18 | BAA01g19740 | A01 | 9735919 | G | A | upstream_gene_variant | MODIFIER | c.-4831C>T| |
S287 |
| 19 | BAA01g19740 | A01 | 9736074 | G | A | upstream_gene_variant | MODIFIER | c.-4986C>T| |
S95 |