| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g18460 | A09 | 11099653 | C | T | missense_variant | MODERATE | c.1180G>A|p.Glu394Lys |
S293 |
| 2 | BAA09g18460 | A09 | 11101406 | C | T | missense_variant | MODERATE | c.226G>A|p.Glu76Lys |
S143 |
| 3 | BAA09g18460 | A09 | 11103277 | G | A | upstream_gene_variant | MODIFIER | c.-1580C>T| |
S4 |
| 4 | BAA09g18460 | A09 | 11103322 | G | A | upstream_gene_variant | MODIFIER | c.-1625C>T| |
S1 |
| 5 | BAA09g18460 | A09 | 11105643 | G | A | upstream_gene_variant | MODIFIER | c.-3946C>T| |
S265 |
| 6 | BAA09g18460 | A09 | 11106037 | C | T | upstream_gene_variant | MODIFIER | c.-4340G>A| |
S69 |
| 7 | BAA09g18460 | A09 | 11106256 | G | A | upstream_gene_variant | MODIFIER | c.-4559C>T| |
S170 S57 |
| 8 | BAA09g18460 | A09 | 11106277 | C | T | upstream_gene_variant | MODIFIER | c.-4580G>A| |
S223 |
| 9 | BAA09g18460 | A09 | 11106316 | C | T | upstream_gene_variant | MODIFIER | c.-4619G>A| |
S13 S278 S279 |
| 10 | BAA09g18460 | A09 | 11106380 | G | A | upstream_gene_variant | MODIFIER | c.-4683C>T| |
S42 |
| 11 | BAA09g18460 | A09 | 11106399 | G | A | upstream_gene_variant | MODIFIER | c.-4702C>T| |
S129 |