| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g43020 | A02 | 35733560 | G | A | upstream_gene_variant | MODIFIER | c.-2571G>A| |
S282 |
| 2 | BAA02g43020 | A02 | 35734731 | C | T | upstream_gene_variant | MODIFIER | c.-1400C>T| |
S216 |
| 3 | BAA02g43020 | A02 | 35736413 | G | A | intron_variant | MODIFIER | c.112+171G>A| |
S5 |
| 4 | BAA02g43020 | A02 | 35736886 | C | T | missense_variant | MODERATE | c.305C>T|p.Ser102Phe |
S61 |
| 5 | BAA02g43020 | A02 | 35738595 | C | T | missense_variant | MODERATE | c.1850C>T|p.Ala617Val |
S117 |
| 6 | BAA02g43020 | A02 | 35739462 | C | T | downstream_gene_variant | MODIFIER | c.*650C>T| |
S39 |
| 7 | BAA02g43020 | A02 | 35740429 | G | A | downstream_gene_variant | MODIFIER | c.*1617G>A| |
S280 |
| 8 | BAA02g43020 | A02 | 35741165 | C | T | downstream_gene_variant | MODIFIER | c.*2353C>T| |
S123 |
| 9 | BAA02g43020 | A02 | 35742568 | C | T | downstream_gene_variant | MODIFIER | c.*3756C>T| |
S181 |