| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g19060 | A02 | 9871212 | G | A | downstream_gene_variant | MODIFIER | c.*4263C>T| |
S296 |
| 2 | BAA02g19060 | A02 | 9876222 | C | T | missense_variant | MODERATE | c.857G>A|p.Gly286Glu |
S275 |
| 3 | BAA02g19060 | A02 | 9877062 | C | T | synonymous_variant | LOW | c.252G>A|p.Glu84Glu |
S177 |
| 4 | BAA02g19060 | A02 | 9879000 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S270 |
| 5 | BAA02g19060 | A02 | 9879183 | G | A | upstream_gene_variant | MODIFIER | c.-1488C>T| |
S76 |
| 6 | BAA02g19060 | A02 | 9879251 | G | A | upstream_gene_variant | MODIFIER | c.-1556C>T| |
S34 |
| 7 | BAA02g19060 | A02 | 9879360 | G | A | upstream_gene_variant | MODIFIER | c.-1665C>T| |
S231 |
| 8 | BAA02g19060 | A02 | 9879489 | G | A | upstream_gene_variant | MODIFIER | c.-1794C>T| |
S282 |
| 9 | BAA02g19060 | A02 | 9879812 | G | A | upstream_gene_variant | MODIFIER | c.-2117C>T| |
S125 |
| 10 | BAA02g19060 | A02 | 9880168 | G | A | upstream_gene_variant | MODIFIER | c.-2473C>T| |
S50 |
| 11 | BAA02g19060 | A02 | 9880503 | G | A | upstream_gene_variant | MODIFIER | c.-2808C>T| |
S153 S213 |
| 12 | BAA02g19060 | A02 | 9880823 | G | A | upstream_gene_variant | MODIFIER | c.-3128C>T| |
S34 |
| 13 | BAA02g19060 | A02 | 9880884 | G | A | upstream_gene_variant | MODIFIER | c.-3189C>T| |
S296 |
| 14 | BAA02g19060 | A02 | 9881622 | G | A | upstream_gene_variant | MODIFIER | c.-3927C>T| |
S41 |
| 15 | BAA02g19060 | A02 | 9881754 | G | A | upstream_gene_variant | MODIFIER | c.-4059C>T| |
S295 |