| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g55910 | A03 | 27605074 | C | T | upstream_gene_variant | MODIFIER | c.-1547C>T| |
S211 S227 |
| 2 | BAA03g55910 | A03 | 27605591 | C | T | upstream_gene_variant | MODIFIER | c.-1030C>T| |
S216 |
| 3 | BAA03g55910 | A03 | 27606362 | G | A | upstream_gene_variant | MODIFIER | c.-259G>A| |
S168 |
| 4 | BAA03g55910 | A03 | 27606524 | C | T | upstream_gene_variant | MODIFIER | c.-97C>T| |
S40 S49 |
| 5 | BAA03g55910 | A03 | 27606706 | C | T | missense_variant | MODERATE | c.86C>T|p.Ala29Val |
S47 |
| 6 | BAA03g55910 | A03 | 27607806 | C | T | synonymous_variant | LOW | c.909C>T|p.Pro303Pro |
S165 |
| 7 | BAA03g55910 | A03 | 27607936 | C | T | stop_gained | HIGH | c.1039C>T|p.Gln347* |
S155 S211 |
| 8 | BAA03g55910 | A03 | 27608070 | T | C | intron_variant | MODIFIER | c.1053+120T>C| |
S5 |
| 9 | BAA03g55910 | A03 | 27609284 | G | A | missense_variant | MODERATE | c.1657G>A|p.Gly553Arg |
S134 S61 |
| 10 | BAA03g55910 | A03 | 27609848 | G | A | downstream_gene_variant | MODIFIER | c.*115G>A| |
S153 S213 |
| 11 | BAA03g55910 | A03 | 27610938 | C | T | downstream_gene_variant | MODIFIER | c.*1205C>T| |
S243 |
| 12 | BAA03g55910 | A03 | 27612583 | C | T | downstream_gene_variant | MODIFIER | c.*2850C>T| |
S105 S106 |