| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g26170 | A07 | 28538269 | G | A | upstream_gene_variant | MODIFIER | c.-779G>A| |
S155 S211 |
| 2 | BAA07g26170 | A07 | 28538811 | C | T | upstream_gene_variant | MODIFIER | c.-237C>T| |
S216 |
| 3 | BAA07g26170 | A07 | 28539015 | C | T | upstream_gene_variant | MODIFIER | c.-33C>T| |
S206 |
| 4 | BAA07g26170 | A07 | 28539043 | C | T | upstream_gene_variant | MODIFIER | c.-5C>T| |
S265 |
| 5 | BAA07g26170 | A07 | 28539680 | C | T | intron_variant | MODIFIER | c.285+60C>T| |
S68 |
| 6 | BAA07g26170 | A07 | 28541094 | C | T | missense_variant | MODERATE | c.1484C>T|p.Ala495Val |
S229 |
| 7 | BAA07g26170 | A07 | 28541412 | T | G | missense_variant | MODERATE | c.1802T>G|p.Leu601Trp |
S53 S56 |
| 8 | BAA07g26170 | A07 | 28541690 | G | A | missense_variant | MODERATE | c.2080G>A|p.Ala694Thr |
S38 |
| 9 | BAA07g26170 | A07 | 28543223 | G | A | downstream_gene_variant | MODIFIER | c.*1267G>A| |
S296 |
| 10 | BAA07g26170 | A07 | 28543316 | C | T | downstream_gene_variant | MODIFIER | c.*1360C>T| |
S247 |
| 11 | BAA07g26170 | A07 | 28543340 | G | A | downstream_gene_variant | MODIFIER | c.*1384G>A| |
S15 S3 |
| 12 | BAA07g26170 | A07 | 28543711 | C | T | downstream_gene_variant | MODIFIER | c.*1755C>T| |
S5 |
| 13 | BAA07g26170 | A07 | 28543943 | G | A | downstream_gene_variant | MODIFIER | c.*1987G>A| |
S72 S78 |