| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g00340 | A01 | 171722 | G | A | downstream_gene_variant | MODIFIER | c.*1718C>T| |
S308 |
| 2 | BAA01g00340 | A01 | 173467 | G | A | synonymous_variant | LOW | c.1251C>T|p.Phe417Phe |
S34 |
| 3 | BAA01g00340 | A01 | 173519 | C | T | missense_variant | MODERATE | c.1199G>A|p.Arg400Lys |
S255 |
| 4 | BAA01g00340 | A01 | 173622 | C | T | missense_variant | MODERATE | c.1096G>A|p.Ala366Thr |
S270 |
| 5 | BAA01g00340 | A01 | 174871 | G | A | missense_variant | MODERATE | c.86C>T|p.Thr29Ile |
S172 S217 |
| 6 | BAA01g00340 | A01 | 178596 | G | A | upstream_gene_variant | MODIFIER | c.-3640C>T| |
S234 |
| 7 | BAA01g00340 | A01 | 178760 | G | A | upstream_gene_variant | MODIFIER | c.-3804C>T| |
S159 S276 S298 |
| 8 | BAA01g00340 | A01 | 179093 | G | A | upstream_gene_variant | MODIFIER | c.-4137C>T| |
S156 |