| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g17890 | A05 | 10156631 | G | A | downstream_gene_variant | MODIFIER | c.*58C>T| |
S82 S92 |
| 2 | BAA05g17890 | A05 | 10157140 | C | T | intron_variant | MODIFIER | c.1141-44G>A| |
S169 |
| 3 | BAA05g17890 | A05 | 10157319 | C | T | missense_variant | MODERATE | c.1039G>A|p.Ala347Thr |
S108 |
| 4 | BAA05g17890 | A05 | 10157434 | G | A | missense_variant | MODERATE | c.1006C>T|p.Pro336Ser |
S170 |
| 5 | BAA05g17890 | A05 | 10157782 | G | A | intron_variant | MODIFIER | c.683-25C>T| |
S78 |
| 6 | BAA05g17890 | A05 | 10158353 | G | A | missense_variant | MODERATE | c.170C>T|p.Ala57Val |
S275 |
| 7 | BAA05g17890 | A05 | 10159987 | C | T | upstream_gene_variant | MODIFIER | c.-1465G>A| |
S136 |
| 8 | BAA05g17890 | A05 | 10160278 | C | T | upstream_gene_variant | MODIFIER | c.-1756G>A| |
S183 S198 |
| 9 | BAA05g17890 | A05 | 10161077 | C | T | upstream_gene_variant | MODIFIER | c.-2555G>A| |
S96 |
| 10 | BAA05g17890 | A05 | 10161475 | C | T | upstream_gene_variant | MODIFIER | c.-2953G>A| |
S100 |
| 11 | BAA05g17890 | A05 | 10161720 | G | A | upstream_gene_variant | MODIFIER | c.-3198C>T| |
S94 |
| 12 | BAA05g17890 | A05 | 10161965 | C | T | upstream_gene_variant | MODIFIER | c.-3443G>A| |
S53 |
| 13 | BAA05g17890 | A05 | 10162206 | G | A | upstream_gene_variant | MODIFIER | c.-3684C>T| |
S192 |
| 14 | BAA05g17890 | A05 | 10163067 | C | T | upstream_gene_variant | MODIFIER | c.-4545G>A| |
S25 |
| 15 | BAA05g17890 | A05 | 10163471 | C | T | upstream_gene_variant | MODIFIER | c.-4949G>A| |
S103 |