| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g58140 | A09 | 57027082 | G | A | downstream_gene_variant | MODIFIER | c.*4343C>T| |
S303 |
| 2 | BAA09g58140 | A09 | 57028160 | C | T | downstream_gene_variant | MODIFIER | c.*3265G>A| |
S13 |
| 3 | BAA09g58140 | A09 | 57028413 | G | A | downstream_gene_variant | MODIFIER | c.*3012C>T| |
S25 |
| 4 | BAA09g58140 | A09 | 57028886 | C | T | downstream_gene_variant | MODIFIER | c.*2539G>A| |
S108 |
| 5 | BAA09g58140 | A09 | 57029064 | C | T | downstream_gene_variant | MODIFIER | c.*2361G>A| |
S281 |
| 6 | BAA09g58140 | A09 | 57029509 | C | T | downstream_gene_variant | MODIFIER | c.*1916G>A| |
S183 |
| 7 | BAA09g58140 | A09 | 57030634 | C | T | downstream_gene_variant | MODIFIER | c.*791G>A| |
S163 |
| 8 | BAA09g58140 | A09 | 57031119 | G | A | downstream_gene_variant | MODIFIER | c.*306C>T| |
S130 |
| 9 | BAA09g58140 | A09 | 57031675 | C | T | missense_variant | MODERATE | c.2876G>A|p.Arg959Lys |
S207 |
| 10 | BAA09g58140 | A09 | 57032782 | G | A | missense_variant | MODERATE | c.1769C>T|p.Ser590Phe |
S113 |
| 11 | BAA09g58140 | A09 | 57034565 | G | A | synonymous_variant | LOW | c.354C>T|p.Arg118Arg |
S15 S3 |
| 12 | BAA09g58140 | A09 | 57036543 | G | A | upstream_gene_variant | MODIFIER | c.-1380C>T| |
S116 |
| 13 | BAA09g58140 | A09 | 57037178 | C | T | upstream_gene_variant | MODIFIER | c.-2015G>A| |
S272 |
| 14 | BAA09g58140 | A09 | 57037393 | G | A | upstream_gene_variant | MODIFIER | c.-2230C>T| |
S165 |
| 15 | BAA09g58140 | A09 | 57037767 | G | A | upstream_gene_variant | MODIFIER | c.-2604C>T| |
S57 |
| 16 | BAA09g58140 | A09 | 57038276 | C | T | upstream_gene_variant | MODIFIER | c.-3113G>A| |
S99 |