| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g19790 | A06 | 10316541 | C | T | upstream_gene_variant | MODIFIER | c.-1818C>T| |
S239 |
| 2 | BAA06g19790 | A06 | 10317060 | C | T | upstream_gene_variant | MODIFIER | c.-1299C>T| |
S286 |
| 3 | BAA06g19790 | A06 | 10317566 | G | A | upstream_gene_variant | MODIFIER | c.-793G>A| |
S28 |
| 4 | BAA06g19790 | A06 | 10318147 | C | T | upstream_gene_variant | MODIFIER | c.-212C>T| |
S260 |
| 5 | BAA06g19790 | A06 | 10318429 | G | A | missense_variant | MODERATE | c.71G>A|p.Gly24Glu |
S122 |
| 6 | BAA06g19790 | A06 | 10318442 | C | T | synonymous_variant | LOW | c.84C>T|p.His28His |
S68 |
| 7 | BAA06g19790 | A06 | 10318677 | G | A | missense_variant | MODERATE | c.319G>A|p.Glu107Lys |
S67 |
| 8 | BAA06g19790 | A06 | 10318714 | C | T | missense_variant | MODERATE | c.356C>T|p.Ala119Val |
S170 |
| 9 | BAA06g19790 | A06 | 10323360 | C | T | downstream_gene_variant | MODIFIER | c.*4213C>T| |
S134 |