| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA04g01380 | A04 | 792376 | C | T | downstream_gene_variant | MODIFIER | c.*2927G>A| |
S129 |
| 2 | BAA04g01380 | A04 | 793225 | C | T | downstream_gene_variant | MODIFIER | c.*2078G>A| |
S202 |
| 3 | BAA04g01380 | A04 | 793501 | G | A | downstream_gene_variant | MODIFIER | c.*1802C>T| |
S47 |
| 4 | BAA04g01380 | A04 | 793677 | C | T | downstream_gene_variant | MODIFIER | c.*1626G>A| |
S263 |
| 5 | BAA04g01380 | A04 | 796770 | G | A | missense_variant | MODERATE | c.548C>T|p.Ala183Val |
S183 S198 |
| 6 | BAA04g01380 | A04 | 798387 | C | T | upstream_gene_variant | MODIFIER | c.-463G>A| |
S28 |
| 7 | BAA04g01380 | A04 | 798413 | C | T | upstream_gene_variant | MODIFIER | c.-489G>A| |
S69 |
| 8 | BAA04g01380 | A04 | 798857 | G | A | upstream_gene_variant | MODIFIER | c.-933C>T| |
S171 S263 |
| 9 | BAA04g01380 | A04 | 799222 | C | A | upstream_gene_variant | MODIFIER | c.-1298G>T| |
S78 |
| 10 | BAA04g01380 | A04 | 799425 | C | T | upstream_gene_variant | MODIFIER | c.-1501G>A| |
S18 |
| 11 | BAA04g01380 | A04 | 799613 | C | T | upstream_gene_variant | MODIFIER | c.-1689G>A| |
S200 |
| 12 | BAA04g01380 | A04 | 800557 | C | T | upstream_gene_variant | MODIFIER | c.-2633G>A| |
S1 S90 |
| 13 | BAA04g01380 | A04 | 800570 | C | A | upstream_gene_variant | MODIFIER | c.-2646G>T| |
S39 |
| 14 | BAA04g01380 | A04 | 800686 | C | T | upstream_gene_variant | MODIFIER | c.-2762G>A| |
S73 S91 |
| 15 | BAA04g01380 | A04 | 800694 | C | T | upstream_gene_variant | MODIFIER | c.-2770G>A| |
S187 |