| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g10080 | A09 | 5559824 | G | A | missense_variant | MODERATE | c.1922C>T|p.Pro641Leu |
S240 |
| 2 | BAA09g10080 | A09 | 5561859 | C | T | missense_variant | MODERATE | c.689G>A|p.Gly230Glu |
S132 S137 S215 S89 |
| 3 | BAA09g10080 | A09 | 5562506 | G | A | missense_variant | MODERATE | c.214C>T|p.Leu72Phe |
S203 |
| 4 | BAA09g10080 | A09 | 5562510 | C | T | synonymous_variant | LOW | c.210G>A|p.Gln70Gln |
S156 |
| 5 | BAA09g10080 | A09 | 5564615 | C | T | upstream_gene_variant | MODIFIER | c.-1539G>A| |
S50 |
| 6 | BAA09g10080 | A09 | 5564819 | G | A | upstream_gene_variant | MODIFIER | c.-1743C>T| |
S265 |
| 7 | BAA09g10080 | A09 | 5564972 | G | A | upstream_gene_variant | MODIFIER | c.-1896C>T| |
S192 |
| 8 | BAA09g10080 | A09 | 5567553 | C | T | upstream_gene_variant | MODIFIER | c.-4477G>A| |
S148 |