| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g10100 | A10 | 11866347 | G | A | synonymous_variant | LOW | c.234C>T|p.Ile78Ile |
S158 |
| 2 | BAA10g10100 | A10 | 11866352 | C | T | missense_variant | MODERATE | c.229G>A|p.Glu77Lys |
S246 |
| 3 | BAA10g10100 | A10 | 11866559 | G | A | synonymous_variant | LOW | c.135C>T|p.Ile45Ile |
S151 S263 |
| 4 | BAA10g10100 | A10 | 11867279 | G | A | upstream_gene_variant | MODIFIER | c.-586C>T| |
S71 |
| 5 | BAA10g10100 | A10 | 11867340 | G | A | upstream_gene_variant | MODIFIER | c.-647C>T| |
S245 |
| 6 | BAA10g10100 | A10 | 11867430 | C | T | upstream_gene_variant | MODIFIER | c.-737G>A| |
S61 |
| 7 | BAA10g10100 | A10 | 11868711 | G | A | upstream_gene_variant | MODIFIER | c.-2018C>T| |
S179 |
| 8 | BAA10g10100 | A10 | 11868765 | C | T | upstream_gene_variant | MODIFIER | c.-2072G>A| |
S269 |
| 9 | BAA10g10100 | A10 | 11869544 | C | T | upstream_gene_variant | MODIFIER | c.-2851G>A| |
S42 |
| 10 | BAA10g10100 | A10 | 11871125 | C | T | upstream_gene_variant | MODIFIER | c.-4432G>A| |
S23 |