| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 167401 | BAA02g13140 | A02 | 5928114 | G | A | upstream_gene_variant | MODIFIER | c.-3025C>T| |
S206 |
| 167402 | BAA02g13140-BAA02g13150 | A02 | 5931242 | C | T | intergenic_region | MODIFIER | n.5931242C>T| |
S71 |
| 167403 | BAA02g13150 | A02 | 5933236 | G | A | upstream_gene_variant | MODIFIER | c.-3071G>A| |
S133 |
| 167404 | BAA02g13150 | A02 | 5937033 | C | T | missense_variant | MODERATE | c.542C>T|p.Pro181Leu |
S158 |
| 167405 | BAA02g13160 | A02 | 5937907 | G | A | upstream_gene_variant | MODIFIER | c.-2454G>A| |
S144 |
| 167406 | BAA02g13160 | A02 | 5938600 | C | T | upstream_gene_variant | MODIFIER | c.-1761C>T| |
S83 S88 |
| 167407 | BAA02g13160 | A02 | 5938827 | C | T | upstream_gene_variant | MODIFIER | c.-1534C>T| |
S182 |
| 167408 | BAA02g13160 | A02 | 5938844 | G | A | upstream_gene_variant | MODIFIER | c.-1517G>A| |
S288 |
| 167409 | BAA02g13160 | A02 | 5939875 | C | T | upstream_gene_variant | MODIFIER | c.-486C>T| |
S38 |
| 167410 | BAA02g13150 | A02 | 5941051 | C | T | downstream_gene_variant | MODIFIER | c.*3702C>T| |
S44 |
| 167411 | BAA02g13160 | A02 | 5941203 | A | T | missense_variant | MODERATE | c.551A>T|p.Tyr184Phe |
S201 |
| 167412 | BAA02g13150 | A02 | 5942193 | C | T | downstream_gene_variant | MODIFIER | c.*4844C>T| |
S117 |
| 167413 | BAA02g13160 | A02 | 5942659 | C | T | downstream_gene_variant | MODIFIER | c.*1155C>T| |
S272 |
| 167414 | BAA02g13160 | A02 | 5943715 | G | A | downstream_gene_variant | MODIFIER | c.*2211G>A| |
S269 |
| 167415 | BAA02g13160 | A02 | 5944816 | G | A | downstream_gene_variant | MODIFIER | c.*3312G>A| |
S228 |
| 167416 | BAA02g13170 | A02 | 5947582 | C | T | downstream_gene_variant | MODIFIER | c.*1228G>A| |
S261 |
| 167417 | BAA02g13170 | A02 | 5947968 | C | T | downstream_gene_variant | MODIFIER | c.*842G>A| |
S54 |
| 167418 | BAA02g13170 | A02 | 5948869 | C | T | missense_variant | MODERATE | c.490G>A|p.Gly164Ser |
S128 |
| 167419 | BAA02g13170 | A02 | 5948980 | C | T | missense_variant | MODERATE | c.379G>A|p.Asp127Asn |
S138 |
| 167420 | BAA02g13170 | A02 | 5949128 | C | T | synonymous_variant | LOW | c.231G>A|p.Glu77Glu |
S79 S84 |
| 167421 | BAA02g13170 | A02 | 5950247 | G | A | upstream_gene_variant | MODIFIER | c.-889C>T| |
S74 |
| 167422 | BAA02g13170 | A02 | 5951815 | C | T | upstream_gene_variant | MODIFIER | c.-2457G>A| |
S130 |
| 167423 | BAA02g13170 | A02 | 5952466 | G | A | upstream_gene_variant | MODIFIER | c.-3108C>T| |
S265 |
| 167424 | BAA02g13170 | A02 | 5953071 | C | T | upstream_gene_variant | MODIFIER | c.-3713G>A| |
S97 |
| 167425 | BAA02g13170 | A02 | 5953097 | G | A | upstream_gene_variant | MODIFIER | c.-3739C>T| |
S10 |