| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g02120 | A09 | 1432907 | C | T | missense_variant | MODERATE | c.152C>T|p.Thr51Ile |
S20 |
| 2 | BAA09g02120 | A09 | 1433572 | G | A | missense_variant | MODERATE | c.568G>A|p.Glu190Lys |
S228 |
| 3 | BAA09g02120 | A09 | 1433678 | G | A | splice_region_variant&intron_variant | LOW | c.669+5G>A| |
S47 |
| 4 | BAA09g02120 | A09 | 1435502 | G | A | synonymous_variant | LOW | c.1536G>A|p.Gly512Gly |
S231 |
| 5 | BAA09g02120 | A09 | 1435892 | C | T | synonymous_variant | LOW | c.1741C>T|p.Leu581Leu |
S94 |
| 6 | BAA09g02120 | A09 | 1435985 | C | T | synonymous_variant | LOW | c.1834C>T|p.Leu612Leu |
S156 |
| 7 | BAA09g02120 | A09 | 1439135 | C | T | downstream_gene_variant | MODIFIER | c.*2602C>T| |
S138 S94 |