| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164651 | BAA02g11030 | A02 | 4976917 | G | A | upstream_gene_variant | MODIFIER | c.-17C>T| |
S68 |
| 164652 | BAA02g11030 | A02 | 4977176 | G | A | upstream_gene_variant | MODIFIER | c.-276C>T| |
S184 |
| 164653 | BAA02g11030 | A02 | 4977376 | C | T | upstream_gene_variant | MODIFIER | c.-476G>A| |
S192 |
| 164654 | BAA02g11030 | A02 | 4977435 | G | A | upstream_gene_variant | MODIFIER | c.-535C>T| |
S294 |
| 164655 | BAA02g11030 | A02 | 4977565 | G | A | upstream_gene_variant | MODIFIER | c.-665C>T| |
S298 |
| 164656 | BAA02g11040 | A02 | 4983232 | G | A | downstream_gene_variant | MODIFIER | c.*1205C>T| |
S87 |
| 164657 | BAA02g11040 | A02 | 4983639 | A | T | downstream_gene_variant | MODIFIER | c.*798T>A| |
S68 |
| 164658 | BAA02g11040 | A02 | 4985474 | G | A | missense_variant | MODERATE | c.626C>T|p.Ala209Val |
S288 |
| 164659 | BAA02g11040 | A02 | 4986269 | G | A | missense_variant | MODERATE | c.253C>T|p.Pro85Ser |
S168 |
| 164660 | BAA02g11040 | A02 | 4987375 | G | A | upstream_gene_variant | MODIFIER | c.-854C>T| |
S50 |
| 164661 | BAA02g11040 | A02 | 4988786 | G | A | upstream_gene_variant | MODIFIER | c.-2265C>T| |
S57 |
| 164662 | BAA02g11050 | A02 | 4990318 | G | A | synonymous_variant | LOW | c.144C>T|p.Leu48Leu |
S105 S106 |
| 164663 | BAA02g11040 | A02 | 4990419 | C | T | upstream_gene_variant | MODIFIER | c.-3898G>A| |
S18 |
| 164664 | BAA02g11040 | A02 | 4990485 | G | A | upstream_gene_variant | MODIFIER | c.-3964C>T| |
S5 |
| 164665 | BAA02g11040 | A02 | 4991265 | C | T | upstream_gene_variant | MODIFIER | c.-4744G>A| |
S273 |
| 164666 | BAA02g11040 | A02 | 4991325 | C | T | upstream_gene_variant | MODIFIER | c.-4804G>A| |
S209 |
| 164667 | BAA02g11040 | A02 | 4991460 | C | T | upstream_gene_variant | MODIFIER | c.-4939G>A| |
S241 |
| 164668 | BAA02g11040 | A02 | 4991493 | G | A | upstream_gene_variant | MODIFIER | c.-4972C>T| |
S166 |
| 164669 | BAA02g11050 | A02 | 4991765 | C | T | upstream_gene_variant | MODIFIER | c.-1061G>A| |
S186 |
| 164670 | BAA02g11050 | A02 | 4993338 | C | T | upstream_gene_variant | MODIFIER | c.-2634G>A| |
S5 |
| 164671 | BAA02g11050 | A02 | 4993621 | G | A | upstream_gene_variant | MODIFIER | c.-2917C>T| |
S35 |
| 164672 | BAA02g11060 | A02 | 4993681 | C | T | missense_variant | MODERATE | c.170C>T|p.Pro57Leu |
S42 |
| 164673 | BAA02g11050 | A02 | 4994901 | C | T | upstream_gene_variant | MODIFIER | c.-4197G>A| |
S94 |
| 164674 | BAA02g11050 | A02 | 4995202 | G | A | upstream_gene_variant | MODIFIER | c.-4498C>T| |
S192 |
| 164675 | BAA02g11050 | A02 | 4995281 | C | T | upstream_gene_variant | MODIFIER | c.-4577G>A| |
S192 |