| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 175651 | BAA02g17940 | A02 | 9010517 | G | A | upstream_gene_variant | MODIFIER | c.-1322G>A| |
S289 S290 |
| 175652 | BAA02g17940 | A02 | 9010667 | C | T | upstream_gene_variant | MODIFIER | c.-1172C>T| |
S180 |
| 175653 | BAA02g17930 | A02 | 9011981 | C | T | upstream_gene_variant | MODIFIER | c.-551G>A| |
S8 |
| 175654 | BAA02g17940 | A02 | 9012115 | C | T | synonymous_variant | LOW | c.141C>T|p.Tyr47Tyr |
S104 S52 |
| 175655 | BAA02g17940 | A02 | 9012336 | G | A | synonymous_variant | LOW | c.282G>A|p.Leu94Leu |
S86 |
| 175656 | BAA02g17940 | A02 | 9012383 | C | T | missense_variant | MODERATE | c.329C>T|p.Ser110Phe |
S180 |
| 175657 | BAA02g17930 | A02 | 9013558 | G | A | upstream_gene_variant | MODIFIER | c.-2128C>T| |
S59 |
| 175658 | BAA02g17930 | A02 | 9014478 | G | A | upstream_gene_variant | MODIFIER | c.-3048C>T| |
S86 |
| 175659 | BAA02g17930 | A02 | 9014572 | G | A | upstream_gene_variant | MODIFIER | c.-3142C>T| |
S176 |
| 175660 | BAA02g17930 | A02 | 9014581 | C | T | upstream_gene_variant | MODIFIER | c.-3151G>A| |
S273 |
| 175661 | BAA02g17930 | A02 | 9015290 | G | A | upstream_gene_variant | MODIFIER | c.-3860C>T| |
S95 |
| 175662 | BAA02g17930 | A02 | 9015544 | G | A | upstream_gene_variant | MODIFIER | c.-4114C>T| |
S299 |
| 175663 | BAA02g17930 | A02 | 9015644 | G | A | upstream_gene_variant | MODIFIER | c.-4214C>T| |
S190 |
| 175664 | BAA02g17930 | A02 | 9016298 | C | T | upstream_gene_variant | MODIFIER | c.-4868G>A| |
S87 |
| 175665 | BAA02g17940 | A02 | 9016726 | G | A | downstream_gene_variant | MODIFIER | c.*4138G>A| |
S82 S92 |
| 175666 | BAA02g17950 | A02 | 9016968 | G | A | missense_variant | MODERATE | c.367C>T|p.Pro123Ser |
S34 |
| 175667 | BAA02g17940 | A02 | 9017284 | G | A | downstream_gene_variant | MODIFIER | c.*4696G>A| |
S148 |
| 175668 | BAA02g17940 | A02 | 9017417 | G | A | downstream_gene_variant | MODIFIER | c.*4829G>A| |
S297 |
| 175669 | BAA02g17950 | A02 | 9017807 | C | T | missense_variant | MODERATE | c.145G>A|p.Val49Ile |
S211 S227 |
| 175670 | BAA02g17950 | A02 | 9017948 | G | A | synonymous_variant | LOW | c.4C>T|p.Leu2Leu |
S172 S217 |
| 175671 | BAA02g17950 | A02 | 9018205 | G | A | upstream_gene_variant | MODIFIER | c.-254C>T| |
S105 |
| 175672 | BAA02g17950 | A02 | 9018867 | G | A | upstream_gene_variant | MODIFIER | c.-916C>T| |
S129 |
| 175673 | BAA02g17950 | A02 | 9019796 | G | A | upstream_gene_variant | MODIFIER | c.-1845C>T| |
S57 |
| 175674 | BAA02g17950 | A02 | 9020775 | T | A | upstream_gene_variant | MODIFIER | c.-2824A>T| |
S100 |
| 175675 | BAA02g17950 | A02 | 9020864 | G | A | upstream_gene_variant | MODIFIER | c.-2913C>T| |
S48 |