| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g04460 | A03 | 1888607 | G | A | splice_region_variant&intron_variant | LOW | c.1401+7C>T| |
S13 |
| 2 | BAA03g04460 | A03 | 1889429 | G | A | missense_variant | MODERATE | c.902C>T|p.Ala301Val |
S262 S96 |
| 3 | BAA03g04460 | A03 | 1889937 | G | A | synonymous_variant | LOW | c.726C>T|p.Leu242Leu |
S301 S304 |
| 4 | BAA03g04460 | A03 | 1890774 | T | C | splice_region_variant&intron_variant | LOW | c.267+5A>G| |
S196 |
| 5 | BAA03g04460 | A03 | 1890911 | G | A | synonymous_variant | LOW | c.135C>T|p.Ala45Ala |
S25 |
| 6 | BAA03g04460 | A03 | 1893703 | C | T | upstream_gene_variant | MODIFIER | c.-2658G>A| |
S32 |
| 7 | BAA03g04460 | A03 | 1893959 | C | T | upstream_gene_variant | MODIFIER | c.-2914G>A| |
S163 |
| 8 | BAA03g04460 | A03 | 1894812 | C | T | upstream_gene_variant | MODIFIER | c.-3767G>A| |
S140 |