| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g37260 | A09 | 45406993 | C | T | upstream_gene_variant | MODIFIER | c.-4911C>T| |
S303 |
| 2 | BAA09g37260 | A09 | 45407748 | C | T | upstream_gene_variant | MODIFIER | c.-4156C>T| |
S237 |
| 3 | BAA09g37260 | A09 | 45407827 | G | A | upstream_gene_variant | MODIFIER | c.-4077G>A| |
S132 S137 S215 |
| 4 | BAA09g37260 | A09 | 45412137 | T | G | synonymous_variant | LOW | c.234T>G|p.Arg78Arg |
S121 S129 S133 S155 S158 S159 S164 S205 S211 S230 S231 S252 S291 S302 S37 S51 S61 S70 S93 |
| 5 | BAA09g37260 | A09 | 45412152 | C | T | synonymous_variant | LOW | c.249C>T|p.Arg83Arg |
S139 |
| 6 | BAA09g37260 | A09 | 45412422 | G | A | missense_variant | MODERATE | c.280G>A|p.Gly94Arg |
S238 |
| 7 | BAA09g37260 | A09 | 45412516 | G | A | missense_variant | MODERATE | c.374G>A|p.Cys125Tyr |
S162 |
| 8 | BAA09g37260 | A09 | 45413228 | C | T | missense_variant | MODERATE | c.886C>T|p.Leu296Phe |
S180 |