| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g41390 | A01 | 27517928 | G | A | upstream_gene_variant | MODIFIER | c.-4391G>A| |
S224 |
| 2 | BAA01g41390 | A01 | 27517995 | C | T | upstream_gene_variant | MODIFIER | c.-4324C>T| |
S159 S243 |
| 3 | BAA01g41390 | A01 | 27518723 | G | A | upstream_gene_variant | MODIFIER | c.-3596G>A| |
S245 |
| 4 | BAA01g41390 | A01 | 27519626 | G | A | upstream_gene_variant | MODIFIER | c.-2693G>A| |
S13 |
| 5 | BAA01g41390 | A01 | 27519650 | C | T | upstream_gene_variant | MODIFIER | c.-2669C>T| |
S146 |
| 6 | BAA01g41390 | A01 | 27521207 | C | T | upstream_gene_variant | MODIFIER | c.-1112C>T| |
S155 S211 |
| 7 | BAA01g41390 | A01 | 27522387 | C | T | synonymous_variant | LOW | c.69C>T|p.Asn23Asn |
S132 S137 S215 |
| 8 | BAA01g41390 | A01 | 27523328 | C | T | missense_variant | MODERATE | c.235C>T|p.Leu79Phe |
S206 S26 |