| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g42180 | A02 | 35153267 | C | T | missense_variant | MODERATE | c.1367G>A|p.Arg456Lys |
S170 |
| 2 | BAA02g42180 | A02 | 35153319 | G | A | missense_variant | MODERATE | c.1315C>T|p.Pro439Ser |
S35 |
| 3 | BAA02g42180 | A02 | 35154733 | G | A | missense_variant | MODERATE | c.361C>T|p.Pro121Ser |
S196 |
| 4 | BAA02g42180 | A02 | 35155977 | G | A | upstream_gene_variant | MODIFIER | c.-884C>T| |
S152 |
| 5 | BAA02g42180 | A02 | 35157115 | C | T | upstream_gene_variant | MODIFIER | c.-2022G>A| |
S100 |
| 6 | BAA02g42180 | A02 | 35159172 | C | T | upstream_gene_variant | MODIFIER | c.-4079G>A| |
S64 |
| 7 | BAA02g42180 | A02 | 35159877 | C | T | upstream_gene_variant | MODIFIER | c.-4784G>A| |
S63 |
| 8 | BAA02g42180 | A02 | 35159929 | C | T | upstream_gene_variant | MODIFIER | c.-4836G>A| |
S9 |