| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g41120 | A05 | 39426817 | G | A | missense_variant | MODERATE | c.235C>T|p.Arg79Cys |
S130 |
| 2 | BAA05g41120 | A05 | 39427796 | C | T | upstream_gene_variant | MODIFIER | c.-574G>A| |
S120 |
| 3 | BAA05g41120 | A05 | 39428404 | C | T | upstream_gene_variant | MODIFIER | c.-1182G>A| |
S260 |
| 4 | BAA05g41120 | A05 | 39429760 | T | C | upstream_gene_variant | MODIFIER | c.-2538A>G| |
S38 |
| 5 | BAA05g41120 | A05 | 39431366 | C | T | upstream_gene_variant | MODIFIER | c.-4144G>A| |
S15 S2 S3 S34 S38 |
| 6 | BAA05g41120 | A05 | 39431415 | G | A | upstream_gene_variant | MODIFIER | c.-4193C>T| |
S164 |
| 7 | BAA05g41120 | A05 | 39431841 | T | A | upstream_gene_variant | MODIFIER | c.-4619A>T| |
S119 S122 S184 S196 S197 S213 S252 S279 S96 |
| 8 | BAA05g41120 | A05 | 39431983 | A | T | upstream_gene_variant | MODIFIER | c.-4761T>A| |
S136 S178 S184 S286 S79 S96 |