| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g09960 | A01 | 4503396 | C | T | missense_variant&splice_region_variant | MODERATE | c.554G>A|p.Gly185Glu |
S200 |
| 2 | BAA01g09960 | A01 | 4503649 | C | T | missense_variant | MODERATE | c.373G>A|p.Gly125Arg |
S70 |
| 3 | BAA01g09960 | A01 | 4505530 | C | T | upstream_gene_variant | MODIFIER | c.-1100G>A| |
S36 |
| 4 | BAA01g09960 | A01 | 4505534 | C | T | upstream_gene_variant | MODIFIER | c.-1104G>A| |
S82 S92 |
| 5 | BAA01g09960 | A01 | 4506420 | G | A | upstream_gene_variant | MODIFIER | c.-1990C>T| |
S142 |
| 6 | BAA01g09960 | A01 | 4507228 | C | T | upstream_gene_variant | MODIFIER | c.-2798G>A| |
S231 |
| 7 | BAA01g09960 | A01 | 4507887 | C | T | upstream_gene_variant | MODIFIER | c.-3457G>A| |
S160 |
| 8 | BAA01g09960 | A01 | 4508359 | G | A | upstream_gene_variant | MODIFIER | c.-3929C>T| |
S209 |