| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g27830 | A02 | 15681231 | C | T | downstream_gene_variant | MODIFIER | c.*2276G>A| |
S270 |
| 2 | BAA02g27830 | A02 | 15681424 | C | T | downstream_gene_variant | MODIFIER | c.*2083G>A| |
S54 |
| 3 | BAA02g27830 | A02 | 15681486 | G | A | downstream_gene_variant | MODIFIER | c.*2021C>T| |
S272 |
| 4 | BAA02g27830 | A02 | 15681512 | G | A | downstream_gene_variant | MODIFIER | c.*1995C>T| |
S149 |
| 5 | BAA02g27830 | A02 | 15681637 | C | T | downstream_gene_variant | MODIFIER | c.*1870G>A| |
S265 S39 |
| 6 | BAA02g27830 | A02 | 15681752 | C | T | downstream_gene_variant | MODIFIER | c.*1755G>A| |
S268 |
| 7 | BAA02g27830 | A02 | 15681753 | C | T | downstream_gene_variant | MODIFIER | c.*1754G>A| |
S181 |
| 8 | BAA02g27830 | A02 | 15682175 | G | A | downstream_gene_variant | MODIFIER | c.*1332C>T| |
S217 S248 |
| 9 | BAA02g27830 | A02 | 15683640 | C | T | missense_variant | MODERATE | c.1271G>A|p.Gly424Glu |
S46 |
| 10 | BAA02g27830 | A02 | 15684079 | C | T | missense_variant | MODERATE | c.832G>A|p.Asp278Asn |
S63 |
| 11 | BAA02g27830 | A02 | 15684094 | C | T | missense_variant | MODERATE | c.817G>A|p.Gly273Ser |
S77 S82 |
| 12 | BAA02g27830 | A02 | 15684321 | G | A | missense_variant | MODERATE | c.590C>T|p.Thr197Ile |
S38 |
| 13 | BAA02g27830 | A02 | 15684521 | G | A | synonymous_variant | LOW | c.390C>T|p.Asn130Asn |
S160 |
| 14 | BAA02g27830 | A02 | 15687363 | G | A | upstream_gene_variant | MODIFIER | c.-2453C>T| |
S86 |
| 15 | BAA02g27830 | A02 | 15688841 | G | A | upstream_gene_variant | MODIFIER | c.-3931C>T| |
S139 |