| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g46780 | A02 | 37919380 | G | A | synonymous_variant | LOW | c.1803C>T|p.Leu601Leu |
S169 |
| 2 | BAA02g46780 | A02 | 37920542 | C | T | missense_variant | MODERATE | c.641G>A|p.Arg214His |
S183 S198 |
| 3 | BAA02g46780 | A02 | 37921275 | T | A | upstream_gene_variant | MODIFIER | c.-28A>T| |
S98 |
| 4 | BAA02g46780 | A02 | 37924793 | G | A | upstream_gene_variant | MODIFIER | c.-3546C>T| |
S144 |
| 5 | BAA02g46780 | A02 | 37924990 | A | G | upstream_gene_variant | MODIFIER | c.-3743T>C| |
S259 |
| 6 | BAA02g46780 | A02 | 37925471 | C | T | upstream_gene_variant | MODIFIER | c.-4224G>A| |
S173 |
| 7 | BAA02g46780 | A02 | 37925907 | C | T | upstream_gene_variant | MODIFIER | c.-4660G>A| |
S15 S3 |