| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g15420 | A09 | 8789355 | C | T | upstream_gene_variant | MODIFIER | c.-2073C>T| |
S133 |
| 2 | BAA09g15420 | A09 | 8789799 | G | A | upstream_gene_variant | MODIFIER | c.-1629G>A| |
S233 |
| 3 | BAA09g15420 | A09 | 8789897 | G | A | upstream_gene_variant | MODIFIER | c.-1531G>A| |
S79 S91 |
| 4 | BAA09g15420 | A09 | 8791223 | G | A | upstream_gene_variant | MODIFIER | c.-205G>A| |
S40 S49 |
| 5 | BAA09g15420 | A09 | 8791253 | G | A | upstream_gene_variant | MODIFIER | c.-175G>A| |
S130 |
| 6 | BAA09g15420 | A09 | 8791993 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.222-1G>A| |
S207 |
| 7 | BAA09g15420 | A09 | 8792377 | C | T | splice_region_variant&intron_variant | LOW | c.433-4C>T| |
S132 S137 |
| 8 | BAA09g15420 | A09 | 8793388 | C | T | missense_variant | MODERATE | c.977C>T|p.Pro326Leu |
S116 |
| 9 | BAA09g15420 | A09 | 8794670 | C | T | missense_variant | MODERATE | c.1853C>T|p.Thr618Met |
S67 |
| 10 | BAA09g15420 | A09 | 8795482 | G | A | synonymous_variant | LOW | c.2325G>A|p.Glu775Glu |
S289 |
| 11 | BAA09g15420 | A09 | 8797647 | G | A | downstream_gene_variant | MODIFIER | c.*1899G>A| |
S262 |
| 12 | BAA09g15420 | A09 | 8797750 | G | A | downstream_gene_variant | MODIFIER | c.*2002G>A| |
S14 |
| 13 | BAA09g15420 | A09 | 8798250 | G | A | downstream_gene_variant | MODIFIER | c.*2502G>A| |
S241 |
| 14 | BAA09g15420 | A09 | 8798444 | G | A | downstream_gene_variant | MODIFIER | c.*2696G>A| |
S182 |
| 15 | BAA09g15420 | A09 | 8800008 | G | A | downstream_gene_variant | MODIFIER | c.*4260G>A| |
S181 |