| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g46110 | A09 | 51031057 | G | A | synonymous_variant | LOW | c.1572C>T|p.Leu524Leu |
S221 |
| 2 | BAA09g46110 | A09 | 51032079 | G | A | missense_variant | MODERATE | c.862C>T|p.Pro288Ser |
S107 |
| 3 | BAA09g46110 | A09 | 51032725 | G | A | missense_variant | MODERATE | c.589C>T|p.Pro197Ser |
S280 |
| 4 | BAA09g46110 | A09 | 51033351 | C | T | missense_variant | MODERATE | c.209G>A|p.Arg70Gln |
S206 S26 |
| 5 | BAA09g46110 | A09 | 51033538 | C | T | missense_variant | MODERATE | c.22G>A|p.Ala8Thr |
S162 |
| 6 | BAA09g46110 | A09 | 51033650 | C | T | upstream_gene_variant | MODIFIER | c.-91G>A| |
S235 |
| 7 | BAA09g46110 | A09 | 51033740 | C | T | upstream_gene_variant | MODIFIER | c.-181G>A| |
S182 |
| 8 | BAA09g46110 | A09 | 51034062 | G | A | upstream_gene_variant | MODIFIER | c.-503C>T| |
S171 S216 |
| 9 | BAA09g46110 | A09 | 51035132 | C | T | upstream_gene_variant | MODIFIER | c.-1573G>A| |
S302 |
| 10 | BAA09g46110 | A09 | 51037198 | C | T | upstream_gene_variant | MODIFIER | c.-3639G>A| |
S295 |