| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g35210 | A02 | 30245543 | C | T | downstream_gene_variant | MODIFIER | c.*906G>A| |
S270 |
| 2 | BAA02g35210 | A02 | 30245592 | C | T | downstream_gene_variant | MODIFIER | c.*857G>A| |
S239 |
| 3 | BAA02g35210 | A02 | 30246367 | T | A | downstream_gene_variant | MODIFIER | c.*82A>T| |
S70 |
| 4 | BAA02g35210 | A02 | 30246476 | C | T | synonymous_variant | LOW | c.1308G>A|p.Arg436Arg |
S212 |
| 5 | BAA02g35210 | A02 | 30247190 | G | A | synonymous_variant | LOW | c.594C>T|p.Asp198Asp |
S269 |
| 6 | BAA02g35210 | A02 | 30247354 | G | A | missense_variant | MODERATE | c.430C>T|p.His144Tyr |
S95 |
| 7 | BAA02g35210 | A02 | 30247518 | G | A | missense_variant | MODERATE | c.266C>T|p.Ala89Val |
S191 |
| 8 | BAA02g35210 | A02 | 30248122 | G | A | upstream_gene_variant | MODIFIER | c.-339C>T| |
S286 |
| 9 | BAA02g35210 | A02 | 30248436 | C | T | upstream_gene_variant | MODIFIER | c.-653G>A| |
S139 |
| 10 | BAA02g35210 | A02 | 30249173 | G | A | upstream_gene_variant | MODIFIER | c.-1390C>T| |
S161 |
| 11 | BAA02g35210 | A02 | 30249918 | G | A | upstream_gene_variant | MODIFIER | c.-2135C>T| |
S10 |
| 12 | BAA02g35210 | A02 | 30250004 | C | T | upstream_gene_variant | MODIFIER | c.-2221G>A| |
S301 S304 |
| 13 | BAA02g35210 | A02 | 30250063 | C | T | upstream_gene_variant | MODIFIER | c.-2280G>A| |
S257 |
| 14 | BAA02g35210 | A02 | 30251790 | C | T | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S201 |
| 15 | BAA02g35210 | A02 | 30251906 | C | T | upstream_gene_variant | MODIFIER | c.-4123G>A| |
S6 |
| 16 | BAA02g35210 | A02 | 30252324 | C | T | upstream_gene_variant | MODIFIER | c.-4541G>A| |
S6 |