| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g09270 | A10 | 11268115 | G | A | synonymous_variant | LOW | c.243C>T|p.Phe81Phe |
S219 S72 |
| 2 | BAA10g09270 | A10 | 11268224 | C | T | missense_variant | MODERATE | c.134G>A|p.Gly45Glu |
S168 |
| 3 | BAA10g09270 | A10 | 11271129 | C | T | upstream_gene_variant | MODIFIER | c.-2203G>A| |
S25 |
| 4 | BAA10g09270 | A10 | 11271343 | G | A | upstream_gene_variant | MODIFIER | c.-2417C>T| |
S148 S210 S30 S31 |
| 5 | BAA10g09270 | A10 | 11271681 | C | T | upstream_gene_variant | MODIFIER | c.-2755G>A| |
S104 S52 |
| 6 | BAA10g09270 | A10 | 11272596 | A | T | upstream_gene_variant | MODIFIER | c.-3670T>A| |
S237 |
| 7 | BAA10g09270 | A10 | 11272610 | C | T | upstream_gene_variant | MODIFIER | c.-3684G>A| |
S287 |
| 8 | BAA10g09270 | A10 | 11273108 | G | A | upstream_gene_variant | MODIFIER | c.-4182C>T| |
S135 S185 S273 S68 |