| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g39770 | A09 | 47213044 | C | T | synonymous_variant | LOW | c.651G>A|p.Val217Val |
S64 |
| 2 | BAA09g39770 | A09 | 47213468 | G | A | synonymous_variant | LOW | c.324C>T|p.Asp108Asp |
S53 |
| 3 | BAA09g39770 | A09 | 47213652 | C | T | missense_variant | MODERATE | c.140G>A|p.Arg47Gln |
S183 S198 |
| 4 | BAA09g39770 | A09 | 47213848 | G | A | upstream_gene_variant | MODIFIER | c.-57C>T| |
S5 |
| 5 | BAA09g39770 | A09 | 47215206 | C | T | upstream_gene_variant | MODIFIER | c.-1415G>A| |
S138 |
| 6 | BAA09g39770 | A09 | 47215861 | C | T | upstream_gene_variant | MODIFIER | c.-2070G>A| |
S33 |
| 7 | BAA09g39770 | A09 | 47216294 | G | A | upstream_gene_variant | MODIFIER | c.-2503C>T| |
S13 |
| 8 | BAA09g39770 | A09 | 47218641 | G | A | upstream_gene_variant | MODIFIER | c.-4850C>T| |
S217 S248 |