| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g23760 | A08 | 17512252 | C | T | downstream_gene_variant | MODIFIER | c.*2978G>A| |
S172 S217 |
| 2 | BAA08g23760 | A08 | 17512268 | C | T | downstream_gene_variant | MODIFIER | c.*2962G>A| |
S33 |
| 3 | BAA08g23760 | A08 | 17516457 | C | T | stop_gained | HIGH | c.1305G>A|p.Trp435* |
S192 |
| 4 | BAA08g23760 | A08 | 17516977 | G | A | missense_variant | MODERATE | c.785C>T|p.Thr262Ile |
S11 S130 |
| 5 | BAA08g23760 | A08 | 17517486 | G | A | synonymous_variant | LOW | c.276C>T|p.Ala92Ala |
S96 |
| 6 | BAA08g23760 | A08 | 17517592 | G | A | missense_variant | MODERATE | c.170C>T|p.Thr57Ile |
S218 |
| 7 | BAA08g23760 | A08 | 17518082 | C | T | upstream_gene_variant | MODIFIER | c.-124G>A| |
S177 |
| 8 | BAA08g23760 | A08 | 17519134 | G | A | upstream_gene_variant | MODIFIER | c.-1176C>T| |
S12 |