| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g21680 | A02 | 11657696 | G | A | downstream_gene_variant | MODIFIER | c.*4194C>T| |
S282 |
| 2 | BAA02g21680 | A02 | 11662070 | C | T | synonymous_variant | LOW | c.477G>A|p.Glu159Glu |
S276 |
| 3 | BAA02g21680 | A02 | 11662588 | C | T | missense_variant | MODERATE | c.187G>A|p.Glu63Lys |
S289 S290 |
| 4 | BAA02g21680 | A02 | 11662758 | G | A | missense_variant | MODERATE | c.17C>T|p.Thr6Ile |
S155 S211 |
| 5 | BAA02g21680 | A02 | 11663585 | G | A | upstream_gene_variant | MODIFIER | c.-811C>T| |
S265 |
| 6 | BAA02g21680 | A02 | 11664000 | C | T | upstream_gene_variant | MODIFIER | c.-1226G>A| |
S178 |
| 7 | BAA02g21680 | A02 | 11664037 | G | A | upstream_gene_variant | MODIFIER | c.-1263C>T| |
S148 S210 S30 S31 |
| 8 | BAA02g21680 | A02 | 11665389 | G | A | upstream_gene_variant | MODIFIER | c.-2615C>T| |
S177 |
| 9 | BAA02g21680 | A02 | 11665515 | T | A | upstream_gene_variant | MODIFIER | c.-2741A>T| |
S138 |
| 10 | BAA02g21680 | A02 | 11666723 | C | T | upstream_gene_variant | MODIFIER | c.-3949G>A| |
S201 |