| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g02290 | A02 | 1027533 | C | T | upstream_gene_variant | MODIFIER | c.-1748C>T| |
S281 |
| 2 | BAA02g02290 | A02 | 1029046 | C | T | upstream_gene_variant | MODIFIER | c.-235C>T| |
S187 |
| 3 | BAA02g02290 | A02 | 1029190 | C | T | upstream_gene_variant | MODIFIER | c.-91C>T| |
S278 |
| 4 | BAA02g02290 | A02 | 1030034 | G | A | missense_variant | MODERATE | c.604G>A|p.Asp202Asn |
S67 |
| 5 | BAA02g02290 | A02 | 1030595 | G | A | splice_donor_variant&intron_variant | HIGH | c.772+1G>A| |
S96 |
| 6 | BAA02g02290 | A02 | 1035330 | G | A | downstream_gene_variant | MODIFIER | c.*3665G>A| |
S157 S166 S167 S236 S262 |
| 7 | BAA02g02290 | A02 | 1035376 | C | T | downstream_gene_variant | MODIFIER | c.*3711C>T| |
S73 |
| 8 | BAA02g02290 | A02 | 1035566 | G | A | downstream_gene_variant | MODIFIER | c.*3901G>A| |
S288 |