| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g16660 | A05 | 9284634 | C | T | synonymous_variant | LOW | c.435G>A|p.Leu145Leu |
S213 |
| 2 | BAA05g16660 | A05 | 9284688 | G | A | synonymous_variant | LOW | c.381C>T|p.Ala127Ala |
S134 |
| 3 | BAA05g16660 | A05 | 9285056 | C | T | missense_variant | MODERATE | c.152G>A|p.Gly51Asp |
S233 |
| 4 | BAA05g16660 | A05 | 9285529 | C | A | upstream_gene_variant | MODIFIER | c.-239G>T| |
S276 S78 |
| 5 | BAA05g16660 | A05 | 9285625 | C | T | upstream_gene_variant | MODIFIER | c.-335G>A| |
S256 |
| 6 | BAA05g16660 | A05 | 9287983 | C | T | upstream_gene_variant | MODIFIER | c.-2693G>A| |
S72 S78 |
| 7 | BAA05g16660 | A05 | 9289240 | C | T | upstream_gene_variant | MODIFIER | c.-3950G>A| |
S206 S26 |
| 8 | BAA05g16660 | A05 | 9289740 | C | T | upstream_gene_variant | MODIFIER | c.-4450G>A| |
S259 |