| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g55140 | A09 | 55423314 | G | A | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S107 |
| 2 | BAA09g55140 | A09 | 55423952 | G | A | missense_variant | MODERATE | c.539C>T|p.Ala180Val |
S178 |
| 3 | BAA09g55140 | A09 | 55424116 | G | A | synonymous_variant | LOW | c.375C>T|p.Ala125Ala |
S70 |
| 4 | BAA09g55140 | A09 | 55424396 | G | A | missense_variant | MODERATE | c.95C>T|p.Thr32Ile |
S193 |
| 5 | BAA09g55140 | A09 | 55424576 | G | A | upstream_gene_variant | MODIFIER | c.-86C>T| |
S113 |
| 6 | BAA09g55140 | A09 | 55425822 | G | A | upstream_gene_variant | MODIFIER | c.-1332C>T| |
S107 |
| 7 | BAA09g55140 | A09 | 55425854 | C | T | upstream_gene_variant | MODIFIER | c.-1364G>A| |
S131 |
| 8 | BAA09g55140 | A09 | 55428596 | C | T | upstream_gene_variant | MODIFIER | c.-4106G>A| |
S50 |