| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g24630 | A10 | 20217277 | G | A | upstream_gene_variant | MODIFIER | c.-324G>A| |
S127 |
| 2 | BAA10g24630 | A10 | 20217303 | G | A | upstream_gene_variant | MODIFIER | c.-298G>A| |
S35 |
| 3 | BAA10g24630 | A10 | 20217852 | C | T | synonymous_variant | LOW | c.252C>T|p.Ala84Ala |
S11 |
| 4 | BAA10g24630 | A10 | 20218053 | C | T | synonymous_variant | LOW | c.453C>T|p.Asp151Asp |
S148 S30 S31 |
| 5 | BAA10g24630 | A10 | 20218461 | G | A | missense_variant | MODERATE | c.779G>A|p.Gly260Glu |
S280 |
| 6 | BAA10g24630 | A10 | 20218499 | G | A | missense_variant | MODERATE | c.817G>A|p.Glu273Lys |
S273 |
| 7 | BAA10g24630 | A10 | 20219168 | C | T | synonymous_variant | LOW | c.1236C>T|p.Ser412Ser |
S204 |
| 8 | BAA10g24630 | A10 | 20219625 | G | A | missense_variant | MODERATE | c.1615G>A|p.Ala539Thr |
S139 |