| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g40440 | A09 | 47589560 | G | A | missense_variant | MODERATE | c.782C>T|p.Ala261Val |
S25 |
| 2 | BAA09g40440 | A09 | 47589855 | C | T | missense_variant | MODERATE | c.487G>A|p.Gly163Ser |
S18 |
| 3 | BAA09g40440 | A09 | 47589956 | C | T | missense_variant | MODERATE | c.386G>A|p.Arg129His |
S95 |
| 4 | BAA09g40440 | A09 | 47590093 | G | A | synonymous_variant | LOW | c.249C>T|p.Cys83Cys |
S48 |
| 5 | BAA09g40440 | A09 | 47590268 | G | A | missense_variant | MODERATE | c.74C>T|p.Ser25Phe |
S144 |
| 6 | BAA09g40440 | A09 | 47590389 | G | A | upstream_gene_variant | MODIFIER | c.-48C>T| |
S40 S49 |
| 7 | BAA09g40440 | A09 | 47590535 | A | G | upstream_gene_variant | MODIFIER | c.-194T>C| |
S117 |
| 8 | BAA09g40440 | A09 | 47590638 | C | T | upstream_gene_variant | MODIFIER | c.-297G>A| |
S124 |
| 9 | BAA09g40440 | A09 | 47591265 | C | T | upstream_gene_variant | MODIFIER | c.-924G>A| |
S80 |
| 10 | BAA09g40440 | A09 | 47591322 | C | T | upstream_gene_variant | MODIFIER | c.-981G>A| |
S240 |
| 11 | BAA09g40440 | A09 | 47591583 | G | A | upstream_gene_variant | MODIFIER | c.-1242C>T| |
S4 |
| 12 | BAA09g40440 | A09 | 47592125 | G | A | upstream_gene_variant | MODIFIER | c.-1784C>T| |
S150 |
| 13 | BAA09g40440 | A09 | 47592308 | G | A | upstream_gene_variant | MODIFIER | c.-1967C>T| |
S84 |
| 14 | BAA09g40440 | A09 | 47592804 | C | T | upstream_gene_variant | MODIFIER | c.-2463G>A| |
S18 |
| 15 | BAA09g40440 | A09 | 47594789 | C | T | upstream_gene_variant | MODIFIER | c.-4448G>A| |
S240 |