| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 172351 | BAA02g16170-BAA02g16180 | A02 | 7886531 | G | A | intergenic_region | MODIFIER | n.7886531G>A| |
S279 |
| 172352 | BAA02g16170-BAA02g16180 | A02 | 7886648 | G | A | intergenic_region | MODIFIER | n.7886648G>A| |
S257 |
| 172353 | BAA02g16170-BAA02g16180 | A02 | 7886929 | C | T | intergenic_region | MODIFIER | n.7886929C>T| |
S275 |
| 172354 | BAA02g16170-BAA02g16180 | A02 | 7886948 | C | T | intergenic_region | MODIFIER | n.7886948C>T| |
S244 |
| 172355 | BAA02g16170-BAA02g16180 | A02 | 7887020 | C | T | intergenic_region | MODIFIER | n.7887020C>T| |
S181 |
| 172356 | BAA02g16180 | A02 | 7887391 | G | A | downstream_gene_variant | MODIFIER | c.*4747C>T| |
S279 |
| 172357 | BAA02g16180 | A02 | 7888483 | C | T | downstream_gene_variant | MODIFIER | c.*3655G>A| |
S128 |
| 172358 | BAA02g16180 | A02 | 7889388 | C | T | downstream_gene_variant | MODIFIER | c.*2750G>A| |
S8 |
| 172359 | BAA02g16180 | A02 | 7890077 | C | T | downstream_gene_variant | MODIFIER | c.*2061G>A| |
S105 S106 |
| 172360 | BAA02g16180 | A02 | 7891788 | C | T | downstream_gene_variant | MODIFIER | c.*350G>A| |
S103 |
| 172361 | BAA02g16180 | A02 | 7892873 | G | A | missense_variant | MODERATE | c.994C>T|p.Pro332Ser |
S297 |
| 172362 | BAA02g16180 | A02 | 7893281 | C | T | synonymous_variant | LOW | c.822G>A|p.Gln274Gln |
S244 |
| 172363 | BAA02g16190 | A02 | 7893765 | G | A | downstream_gene_variant | MODIFIER | c.*2023C>T| |
S36 |
| 172364 | BAA02g16180 | A02 | 7894056 | G | A | synonymous_variant | LOW | c.423C>T|p.Leu141Leu |
S287 |
| 172365 | BAA02g16180 | A02 | 7895569 | G | A | upstream_gene_variant | MODIFIER | c.-844C>T| |
S286 |
| 172366 | BAA02g16190 | A02 | 7896015 | C | T | missense_variant | MODERATE | c.751G>A|p.Val251Met |
S112 |
| 172367 | BAA02g16190 | A02 | 7896117 | C | T | missense_variant | MODERATE | c.649G>A|p.Gly217Ser |
S174 |
| 172368 | BAA02g16190 | A02 | 7896164 | C | T | missense_variant | MODERATE | c.602G>A|p.Gly201Glu |
S174 |
| 172369 | BAA02g16190 | A02 | 7896479 | G | A | missense_variant | MODERATE | c.287C>T|p.Ser96Phe |
S36 |
| 172370 | BAA02g16180 | A02 | 7896770 | G | A | upstream_gene_variant | MODIFIER | c.-2045C>T| |
S148 S30 S31 |
| 172371 | BAA02g16200 | A02 | 7896915 | G | A | missense_variant | MODERATE | c.1784C>T|p.Ser595Phe |
S159 S243 |
| 172372 | BAA02g16180 | A02 | 7897922 | C | T | upstream_gene_variant | MODIFIER | c.-3197G>A| |
S261 |
| 172373 | BAA02g16200 | A02 | 7899940 | C | T | missense_variant | MODERATE | c.34G>A|p.Asp12Asn |
S205 |
| 172374 | BAA02g16200 | A02 | 7899961 | G | A | synonymous_variant | LOW | c.13C>T|p.Leu5Leu |
S237 |
| 172375 | BAA02g16190 | A02 | 7900278 | C | T | upstream_gene_variant | MODIFIER | c.-3513G>A| |
S240 |