| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g35490 | A08 | 22565786 | C | T | missense_variant | MODERATE | c.242C>T|p.Ala81Val |
S138 |
| 2 | BAA08g35490 | A08 | 22565886 | C | T | synonymous_variant | LOW | c.342C>T|p.Leu114Leu |
S176 |
| 3 | BAA08g35490 | A08 | 22566216 | G | A | missense_variant | MODERATE | c.672G>A|p.Met224Ile |
S273 |
| 4 | BAA08g35490 | A08 | 22566321 | C | T | synonymous_variant | LOW | c.777C>T|p.Leu259Leu |
S166 |
| 5 | BAA08g35490 | A08 | 22566556 | C | T | missense_variant | MODERATE | c.1012C>T|p.Pro338Ser |
S171 |
| 6 | BAA08g35490 | A08 | 22567337 | G | A | missense_variant | MODERATE | c.1793G>A|p.Arg598Lys |
S128 |
| 7 | BAA08g35490 | A08 | 22567391 | G | A | missense_variant | MODERATE | c.1847G>A|p.Gly616Glu |
S281 |
| 8 | BAA08g35490 | A08 | 22567710 | G | A | synonymous_variant | LOW | c.2166G>A|p.Glu722Glu |
S272 |