| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g29490 | A05 | 32955427 | C | T | upstream_gene_variant | MODIFIER | c.-3264C>T| |
S8 |
| 2 | BAA05g29490 | A05 | 32955556 | C | T | upstream_gene_variant | MODIFIER | c.-3135C>T| |
S287 |
| 3 | BAA05g29490 | A05 | 32955720 | C | T | upstream_gene_variant | MODIFIER | c.-2971C>T| |
S230 |
| 4 | BAA05g29490 | A05 | 32955904 | C | T | upstream_gene_variant | MODIFIER | c.-2787C>T| |
S207 |
| 5 | BAA05g29490 | A05 | 32956027 | C | T | upstream_gene_variant | MODIFIER | c.-2664C>T| |
S72 S78 |
| 6 | BAA05g29490 | A05 | 32959062 | C | T | missense_variant | MODERATE | c.199C>T|p.Leu67Phe |
S261 |
| 7 | BAA05g29490 | A05 | 32963266 | C | T | downstream_gene_variant | MODIFIER | c.*4199C>T| |
S81 |
| 8 | BAA05g29490 | A05 | 32963680 | C | T | downstream_gene_variant | MODIFIER | c.*4613C>T| |
S268 |
| 9 | BAA05g29490 | A05 | 32963951 | G | A | downstream_gene_variant | MODIFIER | c.*4884G>A| |
S238 |