| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g31860 | A08 | 21081382 | G | A | upstream_gene_variant | MODIFIER | c.-4946G>A| |
S55 |
| 2 | BAA08g31860 | A08 | 21081936 | G | A | upstream_gene_variant | MODIFIER | c.-4392G>A| |
S217 |
| 3 | BAA08g31860 | A08 | 21082276 | C | T | upstream_gene_variant | MODIFIER | c.-4052C>T| |
S231 |
| 4 | BAA08g31860 | A08 | 21082644 | G | A | upstream_gene_variant | MODIFIER | c.-3684G>A| |
S221 |
| 5 | BAA08g31860 | A08 | 21082900 | C | T | upstream_gene_variant | MODIFIER | c.-3428C>T| |
S286 |
| 6 | BAA08g31860 | A08 | 21083316 | G | A | upstream_gene_variant | MODIFIER | c.-3012G>A| |
S122 S276 |
| 7 | BAA08g31860 | A08 | 21085064 | C | T | upstream_gene_variant | MODIFIER | c.-1264C>T| |
S302 |
| 8 | BAA08g31860 | A08 | 21085709 | C | T | upstream_gene_variant | MODIFIER | c.-619C>T| |
S213 |
| 9 | BAA08g31860 | A08 | 21087281 | T | A | missense_variant | MODERATE | c.755T>A|p.Leu252His |
S59 |
| 10 | BAA08g31860 | A08 | 21088028 | C | T | downstream_gene_variant | MODIFIER | c.*335C>T| |
S174 |
| 11 | BAA08g31860 | A08 | 21090269 | G | A | downstream_gene_variant | MODIFIER | c.*2576G>A| |
S42 |