| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g17710 | A09 | 10660677 | G | A | missense_variant | MODERATE | c.440C>T|p.Ser147Phe |
S159 S243 S299 |
| 2 | BAA09g17710 | A09 | 10660800 | C | T | missense_variant | MODERATE | c.317G>A|p.Gly106Glu |
S161 |
| 3 | BAA09g17710 | A09 | 10661871 | C | T | upstream_gene_variant | MODIFIER | c.-690G>A| |
S200 |
| 4 | BAA09g17710 | A09 | 10662871 | G | A | upstream_gene_variant | MODIFIER | c.-1690C>T| |
S249 |
| 5 | BAA09g17710 | A09 | 10663716 | C | T | upstream_gene_variant | MODIFIER | c.-2535G>A| |
S148 S210 |
| 6 | BAA09g17710 | A09 | 10663994 | G | A | upstream_gene_variant | MODIFIER | c.-2813C>T| |
S70 |
| 7 | BAA09g17710 | A09 | 10664320 | G | A | upstream_gene_variant | MODIFIER | c.-3139C>T| |
S88 |
| 8 | BAA09g17710 | A09 | 10665765 | G | A | upstream_gene_variant | MODIFIER | c.-4584C>T| |
S38 |
| 9 | BAA09g17710 | A09 | 10666130 | C | T | upstream_gene_variant | MODIFIER | c.-4949G>A| |
S36 |