| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g26110 | A01 | 14496486 | C | T | upstream_gene_variant | MODIFIER | c.-4086C>T| |
S153 |
| 2 | BAA01g26110 | A01 | 14499104 | G | A | upstream_gene_variant | MODIFIER | c.-1468G>A| |
S245 |
| 3 | BAA01g26110 | A01 | 14499302 | G | A | upstream_gene_variant | MODIFIER | c.-1270G>A| |
S13 |
| 4 | BAA01g26110 | A01 | 14499694 | G | A | upstream_gene_variant | MODIFIER | c.-878G>A| |
S238 |
| 5 | BAA01g26110 | A01 | 14500015 | G | A | upstream_gene_variant | MODIFIER | c.-557G>A| |
S245 |
| 6 | BAA01g26110 | A01 | 14502013 | G | A | synonymous_variant | LOW | c.1086G>A|p.Arg362Arg |
S105 S106 |
| 7 | BAA01g26110 | A01 | 14502145 | C | T | synonymous_variant | LOW | c.1218C>T|p.Tyr406Tyr |
S65 |
| 8 | BAA01g26110 | A01 | 14502724 | G | A | missense_variant | MODERATE | c.1714G>A|p.Asp572Asn |
S241 |
| 9 | BAA01g26110 | A01 | 14503925 | G | A | downstream_gene_variant | MODIFIER | c.*1178G>A| |
S153 |