| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g05960 | A09 | 3350601 | G | A | upstream_gene_variant | MODIFIER | c.-4560G>A| |
S302 |
| 2 | BAA09g05960 | A09 | 3352922 | C | T | upstream_gene_variant | MODIFIER | c.-2239C>T| |
S61 |
| 3 | BAA09g05960 | A09 | 3353768 | C | T | upstream_gene_variant | MODIFIER | c.-1393C>T| |
S35 |
| 4 | BAA09g05960 | A09 | 3354059 | G | A | upstream_gene_variant | MODIFIER | c.-1102G>A| |
S247 |
| 5 | BAA09g05960 | A09 | 3354475 | C | T | upstream_gene_variant | MODIFIER | c.-686C>T| |
S210 S225 |
| 6 | BAA09g05960 | A09 | 3354710 | G | A | upstream_gene_variant | MODIFIER | c.-451G>A| |
S274 |
| 7 | BAA09g05960 | A09 | 3355201 | A | C | missense_variant | MODERATE | c.41A>C|p.Asn14Thr |
S111 S172 S26 S276 S283 S63 S9 |
| 8 | BAA09g05960 | A09 | 3356506 | G | A | downstream_gene_variant | MODIFIER | c.*51G>A| |
S295 |
| 9 | BAA09g05960 | A09 | 3357116 | G | T | downstream_gene_variant | MODIFIER | c.*661G>T| |
S122 S124 S149 S153 S184 S196 S205 S218 S220 S222 S228 S262 S264 S268 S289 S40 S73 S79 S95 |
| 10 | BAA09g05960 | A09 | 3357124 | C | A | downstream_gene_variant | MODIFIER | c.*669C>A| |
S124 S149 S184 S185 S205 S218 S220 S222 S228 S247 S262 S264 S73 |