| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g08940 | A07 | 17857428 | C | T | missense_variant | MODERATE | c.596G>A|p.Gly199Asp |
S249 |
| 2 | BAA07g08940 | A07 | 17857466 | G | A | synonymous_variant | LOW | c.558C>T|p.Tyr186Tyr |
S182 |
| 3 | BAA07g08940 | A07 | 17858041 | G | A | synonymous_variant | LOW | c.147C>T|p.Leu49Leu |
S44 |
| 4 | BAA07g08940 | A07 | 17858359 | C | T | upstream_gene_variant | MODIFIER | c.-172G>A| |
S86 |
| 5 | BAA07g08940 | A07 | 17858494 | C | T | upstream_gene_variant | MODIFIER | c.-307G>A| |
S46 |
| 6 | BAA07g08940 | A07 | 17860885 | C | T | upstream_gene_variant | MODIFIER | c.-2698G>A| |
S94 |
| 7 | BAA07g08940 | A07 | 17861289 | G | A | upstream_gene_variant | MODIFIER | c.-3102C>T| |
S178 |
| 8 | BAA07g08940 | A07 | 17862412 | C | T | upstream_gene_variant | MODIFIER | c.-4225G>A| |
S181 |