| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g51170 | A09 | 53663181 | C | T | missense_variant | MODERATE | c.809G>A|p.Gly270Glu |
S174 |
| 2 | BAA09g51170 | A09 | 53663929 | G | A | missense_variant | MODERATE | c.61C>T|p.Leu21Phe |
S130 |
| 3 | BAA09g51170 | A09 | 53663932 | G | A | missense_variant | MODERATE | c.58C>T|p.Pro20Ser |
S192 |
| 4 | BAA09g51170 | A09 | 53664181 | C | T | upstream_gene_variant | MODIFIER | c.-192G>A| |
S223 |
| 5 | BAA09g51170 | A09 | 53664983 | C | T | upstream_gene_variant | MODIFIER | c.-994G>A| |
S301 S304 |
| 6 | BAA09g51170 | A09 | 53665216 | C | T | upstream_gene_variant | MODIFIER | c.-1227G>A| |
S136 |
| 7 | BAA09g51170 | A09 | 53665396 | T | G | upstream_gene_variant | MODIFIER | c.-1407A>C| |
S276 |
| 8 | BAA09g51170 | A09 | 53665485 | C | T | upstream_gene_variant | MODIFIER | c.-1496G>A| |
S195 |
| 9 | BAA09g51170 | A09 | 53665532 | G | A | upstream_gene_variant | MODIFIER | c.-1543C>T| |
S276 |
| 10 | BAA09g51170 | A09 | 53666533 | C | T | upstream_gene_variant | MODIFIER | c.-2544G>A| |
S269 |
| 11 | BAA09g51170 | A09 | 53666709 | C | T | upstream_gene_variant | MODIFIER | c.-2720G>A| |
S294 |
| 12 | BAA09g51170 | A09 | 53668214 | G | A | upstream_gene_variant | MODIFIER | c.-4225C>T| |
S47 |