| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g24860 | A10 | 20332881 | C | T | synonymous_variant | LOW | c.1053G>A|p.Glu351Glu |
S210 S225 |
| 2 | BAA10g24860 | A10 | 20332883 | C | T | missense_variant | MODERATE | c.1051G>A|p.Glu351Lys |
S87 |
| 3 | BAA10g24860 | A10 | 20332954 | G | A | missense_variant | MODERATE | c.980C>T|p.Pro327Leu |
S132 S137 S215 S237 S89 |
| 4 | BAA10g24860 | A10 | 20332977 | C | T | synonymous_variant | LOW | c.957G>A|p.Thr319Thr |
S221 |
| 5 | BAA10g24860 | A10 | 20333851 | G | A | synonymous_variant | LOW | c.288C>T|p.Ser96Ser |
S293 |
| 6 | BAA10g24860 | A10 | 20334091 | C | T | synonymous_variant | LOW | c.48G>A|p.Leu16Leu |
S140 |
| 7 | BAA10g24860 | A10 | 20336964 | G | A | upstream_gene_variant | MODIFIER | c.-2668C>T| |
S278 |
| 8 | BAA10g24860 | A10 | 20338215 | C | T | upstream_gene_variant | MODIFIER | c.-3919G>A| |
S195 |
| 9 | BAA10g24860 | A10 | 20338622 | C | T | upstream_gene_variant | MODIFIER | c.-4326G>A| |
S133 |