| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g25150 | A02 | 13748846 | G | A | upstream_gene_variant | MODIFIER | c.-1530G>A| |
S188 |
| 2 | BAA02g25150 | A02 | 13748895 | G | A | upstream_gene_variant | MODIFIER | c.-1481G>A| |
S162 |
| 3 | BAA02g25150 | A02 | 13750673 | G | A | missense_variant | MODERATE | c.298G>A|p.Asp100Asn |
S13 |
| 4 | BAA02g25150 | A02 | 13750811 | G | A | missense_variant | MODERATE | c.436G>A|p.Glu146Lys |
S122 |
| 5 | BAA02g25150 | A02 | 13750889 | G | A | missense_variant | MODERATE | c.514G>A|p.Asp172Asn |
S269 |
| 6 | BAA02g25150 | A02 | 13751292 | C | T | missense_variant | MODERATE | c.917C>T|p.Pro306Leu |
S82 S92 |
| 7 | BAA02g25150 | A02 | 13751419 | G | A | synonymous_variant | LOW | c.1044G>A|p.Ala348Ala |
S44 |
| 8 | BAA02g25150 | A02 | 13751489 | G | A | missense_variant | MODERATE | c.1114G>A|p.Asp372Asn |
S196 |
| 9 | BAA02g25150 | A02 | 13751500 | G | A | synonymous_variant | LOW | c.1125G>A|p.Ser375Ser |
S19 |
| 10 | BAA02g25150 | A02 | 13753360 | C | T | downstream_gene_variant | MODIFIER | c.*1335C>T| |
S144 |
| 11 | BAA02g25150 | A02 | 13753894 | G | A | downstream_gene_variant | MODIFIER | c.*1869G>A| |
S288 |
| 12 | BAA02g25150 | A02 | 13754119 | C | T | downstream_gene_variant | MODIFIER | c.*2094C>T| |
S2 |