| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g02780 | A10 | 1325690 | G | A | missense_variant | MODERATE | c.139G>A|p.Glu47Lys |
S150 |
| 2 | BAA10g02780 | A10 | 1325751 | T | C | missense_variant | MODERATE | c.200T>C|p.Val67Ala |
S226 |
| 3 | BAA10g02780 | A10 | 1327354 | T | C | synonymous_variant | LOW | c.598T>C|p.Leu200Leu |
S197 S210 S225 S229 S247 |
| 4 | BAA10g02780 | A10 | 1327420 | C | T | synonymous_variant | LOW | c.664C>T|p.Leu222Leu |
S246 |
| 5 | BAA10g02780 | A10 | 1327738 | G | A | missense_variant | MODERATE | c.766G>A|p.Gly256Arg |
S289 |
| 6 | BAA10g02780 | A10 | 1329596 | G | A | downstream_gene_variant | MODIFIER | c.*1853G>A| |
S71 |
| 7 | BAA10g02780 | A10 | 1329963 | G | A | downstream_gene_variant | MODIFIER | c.*2220G>A| |
S156 |
| 8 | BAA10g02780 | A10 | 1330569 | C | T | downstream_gene_variant | MODIFIER | c.*2826C>T| |
S139 |