| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g47790 | A03 | 22932958 | G | A | downstream_gene_variant | MODIFIER | c.*1419C>T| |
S31 |
| 2 | BAA03g47790 | A03 | 22933362 | C | T | downstream_gene_variant | MODIFIER | c.*1015G>A| |
S16 |
| 3 | BAA03g47790 | A03 | 22933594 | C | T | downstream_gene_variant | MODIFIER | c.*783G>A| |
S303 |
| 4 | BAA03g47790 | A03 | 22933768 | C | T | downstream_gene_variant | MODIFIER | c.*609G>A| |
S250 |
| 5 | BAA03g47790 | A03 | 22933782 | G | A | downstream_gene_variant | MODIFIER | c.*595C>T| |
S8 |
| 6 | BAA03g47790 | A03 | 22933854 | G | A | downstream_gene_variant | MODIFIER | c.*523C>T| |
S200 |
| 7 | BAA03g47790 | A03 | 22934197 | C | T | downstream_gene_variant | MODIFIER | c.*180G>A| |
S75 S81 |
| 8 | BAA03g47790 | A03 | 22934474 | G | A | missense_variant | MODERATE | c.1175C>T|p.Thr392Ile |
S112 |
| 9 | BAA03g47790 | A03 | 22935548 | C | T | missense_variant | MODERATE | c.101G>A|p.Arg34Lys |
S125 S139 |
| 10 | BAA03g47790 | A03 | 22937959 | G | A | upstream_gene_variant | MODIFIER | c.-2311C>T| |
S162 |
| 11 | BAA03g47790 | A03 | 22938098 | G | A | upstream_gene_variant | MODIFIER | c.-2450C>T| |
S242 |
| 12 | BAA03g47790 | A03 | 22938624 | G | A | upstream_gene_variant | MODIFIER | c.-2976C>T| |
S197 |
| 13 | BAA03g47790 | A03 | 22938717 | G | A | upstream_gene_variant | MODIFIER | c.-3069C>T| |
S9 |