| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g08240 | A02 | 3530940 | G | A | missense_variant | MODERATE | c.1313C>T|p.Ser438Phe |
S205 |
| 2 | BAA02g08240 | A02 | 3531328 | C | T | missense_variant | MODERATE | c.1016G>A|p.Gly339Glu |
S262 |
| 3 | BAA02g08240 | A02 | 3532528 | G | A | splice_region_variant&intron_variant | LOW | c.241-6C>T| |
S119 |
| 4 | BAA02g08240 | A02 | 3533409 | G | A | upstream_gene_variant | MODIFIER | c.-586C>T| |
S209 |
| 5 | BAA02g08240 | A02 | 3534194 | G | A | upstream_gene_variant | MODIFIER | c.-1371C>T| |
S92 |
| 6 | BAA02g08240 | A02 | 3534277 | G | A | upstream_gene_variant | MODIFIER | c.-1454C>T| |
S287 |
| 7 | BAA02g08240 | A02 | 3536486 | C | T | upstream_gene_variant | MODIFIER | c.-3663G>A| |
S268 |
| 8 | BAA02g08240 | A02 | 3536673 | G | A | upstream_gene_variant | MODIFIER | c.-3850C>T| |
S67 |