| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g05120 | A09 | 2982007 | T | A | upstream_gene_variant | MODIFIER | c.-3146T>A| |
S302 |
| 2 | BAA09g05120 | A09 | 2982456 | C | A | upstream_gene_variant | MODIFIER | c.-2697C>A| |
S105 S106 |
| 3 | BAA09g05120 | A09 | 2982892 | G | A | upstream_gene_variant | MODIFIER | c.-2261G>A| |
S174 S216 S27 S39 |
| 4 | BAA09g05120 | A09 | 2983691 | C | T | upstream_gene_variant | MODIFIER | c.-1462C>T| |
S263 |
| 5 | BAA09g05120 | A09 | 2983926 | T | C | upstream_gene_variant | MODIFIER | c.-1227T>C| |
S163 |
| 6 | BAA09g05120 | A09 | 2984361 | G | A | upstream_gene_variant | MODIFIER | c.-792G>A| |
S42 |
| 7 | BAA09g05120 | A09 | 2984557 | G | A | upstream_gene_variant | MODIFIER | c.-596G>A| |
S7 |
| 8 | BAA09g05120 | A09 | 2986001 | C | T | synonymous_variant | LOW | c.510C>T|p.Asp170Asp |
S278 |
| 9 | BAA09g05120 | A09 | 2986369 | G | A | missense_variant | MODERATE | c.712G>A|p.Asp238Asn |
S157 |