| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g29500 | A08 | 20241707 | C | T | missense_variant | MODERATE | c.113C>T|p.Ser38Phe |
S283 |
| 2 | BAA08g29500 | A08 | 20241898 | C | T | stop_gained | HIGH | c.304C>T|p.Gln102* |
S177 |
| 3 | BAA08g29500 | A08 | 20241906 | C | T | synonymous_variant | LOW | c.312C>T|p.Pro104Pro |
S223 |
| 4 | BAA08g29500 | A08 | 20243443 | G | A | missense_variant | MODERATE | c.758G>A|p.Arg253Lys |
S279 |
| 5 | BAA08g29500 | A08 | 20243694 | C | T | missense_variant | MODERATE | c.769C>T|p.Leu257Phe |
S167 |
| 6 | BAA08g29500 | A08 | 20247075 | C | T | downstream_gene_variant | MODIFIER | c.*3229C>T| |
S134 |
| 7 | BAA08g29500 | A08 | 20247244 | G | A | downstream_gene_variant | MODIFIER | c.*3398G>A| |
S46 |
| 8 | BAA08g29500 | A08 | 20248812 | C | T | downstream_gene_variant | MODIFIER | c.*4966C>T| |
S251 |