| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g11550 | A08 | 10216343 | C | T | upstream_gene_variant | MODIFIER | c.-1913C>T| |
S155 S211 |
| 2 | BAA08g11550 | A08 | 10216403 | G | A | upstream_gene_variant | MODIFIER | c.-1853G>A| |
S61 |
| 3 | BAA08g11550 | A08 | 10216583 | G | A | upstream_gene_variant | MODIFIER | c.-1673G>A| |
S274 |
| 4 | BAA08g11550 | A08 | 10218339 | C | T | synonymous_variant | LOW | c.84C>T|p.Val28Val |
S162 |
| 5 | BAA08g11550 | A08 | 10218454 | C | T | missense_variant | MODERATE | c.199C>T|p.Pro67Ser |
S80 |
| 6 | BAA08g11550 | A08 | 10218556 | G | A | missense_variant | MODERATE | c.301G>A|p.Glu101Lys |
S148 S210 |
| 7 | BAA08g11550 | A08 | 10219698 | G | T | synonymous_variant | LOW | c.1125G>T|p.Thr375Thr |
S298 |
| 8 | BAA08g11550 | A08 | 10219898 | C | T | missense_variant | MODERATE | c.1240C>T|p.Pro414Ser |
S186 |
| 9 | BAA08g11550 | A08 | 10220904 | C | T | synonymous_variant | LOW | c.1989C>T|p.Tyr663Tyr |
S168 |
| 10 | BAA08g11550 | A08 | 10221189 | C | T | downstream_gene_variant | MODIFIER | c.*66C>T| |
S148 S210 S30 S31 |
| 11 | BAA08g11550 | A08 | 10222219 | G | A | downstream_gene_variant | MODIFIER | c.*1096G>A| |
S245 |