| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g50490 | A09 | 53348677 | C | T | upstream_gene_variant | MODIFIER | c.-2403C>T| |
S92 |
| 2 | BAA09g50490 | A09 | 53349527 | G | A | upstream_gene_variant | MODIFIER | c.-1553G>A| |
S268 |
| 3 | BAA09g50490 | A09 | 53351230 | C | T | missense_variant | MODERATE | c.151C>T|p.His51Tyr |
S115 |
| 4 | BAA09g50490 | A09 | 53351305 | G | A | missense_variant | MODERATE | c.226G>A|p.Gly76Arg |
|
| 5 | BAA09g50490 | A09 | 53353458 | C | T | downstream_gene_variant | MODIFIER | c.*1845C>T| |
S63 |
| 6 | BAA09g50490 | A09 | 53354480 | G | A | downstream_gene_variant | MODIFIER | c.*2867G>A| |
S271 |
| 7 | BAA09g50490 | A09 | 53355513 | G | A | downstream_gene_variant | MODIFIER | c.*3900G>A| |
S185 |
| 8 | BAA09g50490 | A09 | 53355537 | G | A | downstream_gene_variant | MODIFIER | c.*3924G>A| |
S247 |
| 9 | BAA09g50490 | A09 | 53356428 | C | T | downstream_gene_variant | MODIFIER | c.*4815C>T| |
S158 |