| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g11490 | A08 | 10186031 | G | A | upstream_gene_variant | MODIFIER | c.-4539G>A| |
S109 |
| 2 | BAA08g11490 | A08 | 10186753 | G | A | upstream_gene_variant | MODIFIER | c.-3817G>A| |
S197 |
| 3 | BAA08g11490 | A08 | 10187154 | C | T | upstream_gene_variant | MODIFIER | c.-3416C>T| |
S138 |
| 4 | BAA08g11490 | A08 | 10189178 | C | T | upstream_gene_variant | MODIFIER | c.-1392C>T| |
S185 |
| 5 | BAA08g11490 | A08 | 10189931 | G | A | upstream_gene_variant | MODIFIER | c.-639G>A| |
S34 |
| 6 | BAA08g11490 | A08 | 10190749 | C | T | synonymous_variant | LOW | c.180C>T|p.Phe60Phe |
S144 |
| 7 | BAA08g11490 | A08 | 10191541 | G | A | splice_region_variant&stop_retained_variant | LOW | c.614G>A|p.Ter205Ter |
S35 |
| 8 | BAA08g11490 | A08 | 10194618 | C | T | downstream_gene_variant | MODIFIER | c.*3076C>T| |
S183 S198 |
| 9 | BAA08g11490 | A08 | 10195294 | C | T | downstream_gene_variant | MODIFIER | c.*3752C>T| |
S143 |