| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g17730 | A06 | 9048063 | C | T | missense_variant | MODERATE | c.1144G>A|p.Gly382Arg |
S126 |
| 2 | BAA06g17730 | A06 | 9048868 | G | A | synonymous_variant | LOW | c.831C>T|p.Thr277Thr |
S161 |
| 3 | BAA06g17730 | A06 | 9048974 | G | A | missense_variant | MODERATE | c.725C>T|p.Ala242Val |
S139 |
| 4 | BAA06g17730 | A06 | 9052162 | G | A | upstream_gene_variant | MODIFIER | c.-1320C>T| |
S9 |
| 5 | BAA06g17730 | A06 | 9052220 | C | T | upstream_gene_variant | MODIFIER | c.-1378G>A| |
S296 |
| 6 | BAA06g17730 | A06 | 9052468 | C | T | upstream_gene_variant | MODIFIER | c.-1626G>A| |
S257 |
| 7 | BAA06g17730 | A06 | 9054941 | C | T | upstream_gene_variant | MODIFIER | c.-4099G>A| |
S247 |
| 8 | BAA06g17730 | A06 | 9055685 | C | T | upstream_gene_variant | MODIFIER | c.-4843G>A| |
S267 |