| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g03880 | A01 | 1758136 | C | T | upstream_gene_variant | MODIFIER | c.-3607C>T| |
S25 |
| 2 | BAA01g03880 | A01 | 1758791 | C | T | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S137 S215 |
| 3 | BAA01g03880 | A01 | 1760052 | G | A | upstream_gene_variant | MODIFIER | c.-1691G>A| |
S224 |
| 4 | BAA01g03880 | A01 | 1762124 | C | T | stop_gained | HIGH | c.382C>T|p.Gln128* |
S223 |
| 5 | BAA01g03880 | A01 | 1762555 | C | T | synonymous_variant | LOW | c.813C>T|p.Val271Val |
S257 |
| 6 | BAA01g03880 | A01 | 1764960 | G | A | synonymous_variant | LOW | c.1584G>A|p.Gly528Gly |
S240 |
| 7 | BAA01g03880 | A01 | 1765022 | G | A | missense_variant | MODERATE | c.1646G>A|p.Gly549Glu |
S172 S217 |
| 8 | BAA01g03880 | A01 | 1765375 | G | A | missense_variant | MODERATE | c.1999G>A|p.Gly667Ser |
S289 S290 |