| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 158701 | BAA02g06270 | A02 | 2659763 | C | T | upstream_gene_variant | MODIFIER | c.-4146G>A| |
S37 |
| 158702 | BAA02g06270 | A02 | 2660529 | G | A | upstream_gene_variant | MODIFIER | c.-4912C>T| |
S210 |
| 158703 | BAA02g06290 | A02 | 2661046 | G | A | upstream_gene_variant | MODIFIER | c.-1507G>A| |
S17 |
| 158704 | BAA02g06290 | A02 | 2661467 | G | A | upstream_gene_variant | MODIFIER | c.-1086G>A| |
S34 |
| 158705 | BAA02g06290 | A02 | 2661515 | G | A | upstream_gene_variant | MODIFIER | c.-1038G>A| |
S156 |
| 158706 | BAA02g06290 | A02 | 2661694 | C | T | upstream_gene_variant | MODIFIER | c.-859C>T| |
S159 S188 S276 S299 |
| 158707 | BAA02g06290 | A02 | 2661706 | G | A | upstream_gene_variant | MODIFIER | c.-847G>A| |
S11 |
| 158708 | BAA02g06290 | A02 | 2661875 | C | T | upstream_gene_variant | MODIFIER | c.-678C>T| |
S261 |
| 158709 | BAA02g06290 | A02 | 2661951 | C | T | upstream_gene_variant | MODIFIER | c.-602C>T| |
S257 |
| 158710 | BAA02g06290 | A02 | 2662593 | C | T | missense_variant | MODERATE | c.41C>T|p.Ala14Val |
S13 |
| 158711 | BAA02g06290 | A02 | 2662810 | G | A | synonymous_variant | LOW | c.114G>A|p.Pro38Pro |
S286 |
| 158712 | BAA02g06290 | A02 | 2663163 | G | A | missense_variant | MODERATE | c.467G>A|p.Gly156Glu |
S127 |
| 158713 | BAA02g06280 | A02 | 2663376 | C | T | downstream_gene_variant | MODIFIER | c.*3792C>T| |
S180 |
| 158714 | BAA02g06280 | A02 | 2663448 | G | A | downstream_gene_variant | MODIFIER | c.*3864G>A| |
S5 |
| 158715 | BAA02g06300 | A02 | 2664893 | C | T | upstream_gene_variant | MODIFIER | c.-4970C>T| |
S289 S290 |
| 158716 | BAA02g06300 | A02 | 2665271 | C | T | upstream_gene_variant | MODIFIER | c.-4592C>T| |
S243 |
| 158717 | BAA02g06300 | A02 | 2665459 | G | A | upstream_gene_variant | MODIFIER | c.-4404G>A| |
S125 |
| 158718 | BAA02g06300 | A02 | 2665531 | G | A | upstream_gene_variant | MODIFIER | c.-4332G>A| |
S282 |
| 158719 | BAA02g06300 | A02 | 2666113 | G | A | upstream_gene_variant | MODIFIER | c.-3750G>A| |
S206 S26 |
| 158720 | BAA02g06300 | A02 | 2667152 | C | T | upstream_gene_variant | MODIFIER | c.-2711C>T| |
S65 |
| 158721 | BAA02g06300 | A02 | 2667708 | C | T | upstream_gene_variant | MODIFIER | c.-2155C>T| |
S1 S90 |
| 158722 | BAA02g06300 | A02 | 2667927 | G | A | upstream_gene_variant | MODIFIER | c.-1936G>A| |
S207 |
| 158723 | BAA02g06310 | A02 | 2670197 | G | A | upstream_gene_variant | MODIFIER | c.-2369G>A| |
S164 |
| 158724 | BAA02g06300 | A02 | 2671949 | C | T | missense_variant | MODERATE | c.1459C>T|p.Pro487Ser |
S13 |
| 158725 | BAA02g06300 | A02 | 2673700 | C | T | downstream_gene_variant | MODIFIER | c.*1659C>T| |
S33 |