| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g00550 | A09 | 505939 | G | A | missense_variant | MODERATE | c.1327C>T|p.Pro443Ser |
S107 |
| 2 | BAA09g00550 | A09 | 507028 | G | A | synonymous_variant | LOW | c.810C>T|p.Ile270Ile |
S136 |
| 3 | BAA09g00550 | A09 | 509668 | C | T | upstream_gene_variant | MODIFIER | c.-1312G>A| |
S239 |
| 4 | BAA09g00550 | A09 | 510017 | C | T | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S270 |
| 5 | BAA09g00550 | A09 | 511853 | G | A | upstream_gene_variant | MODIFIER | c.-3497C>T| |
S262 |
| 6 | BAA09g00550 | A09 | 512327 | C | T | upstream_gene_variant | MODIFIER | c.-3971G>A| |
S144 |