| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA04g16840 | A04 | 21133728 | G | A | upstream_gene_variant | MODIFIER | c.-2023G>A| |
S203 |
| 2 | BAA04g16840 | A04 | 21134242 | C | T | upstream_gene_variant | MODIFIER | c.-1509C>T| |
S308 |
| 3 | BAA04g16840 | A04 | 21135316 | C | T | upstream_gene_variant | MODIFIER | c.-435C>T| |
S296 |
| 4 | BAA04g16840 | A04 | 21136204 | C | T | missense_variant | MODERATE | c.454C>T|p.Leu152Phe |
S185 |
| 5 | BAA04g16840 | A04 | 21136209 | G | A | synonymous_variant | LOW | c.459G>A|p.Gly153Gly |
S276 |
| 6 | BAA04g16840 | A04 | 21136299 | C | T | synonymous_variant | LOW | c.549C>T|p.Leu183Leu |
S249 |
| 7 | BAA04g16840 | A04 | 21137079 | G | A | synonymous_variant | LOW | c.1329G>A|p.Pro443Pro |
S261 |
| 8 | BAA04g16840 | A04 | 21137175 | C | T | intron_variant | MODIFIER | c.1399+26C>T| |
S47 |
| 9 | BAA04g16840 | A04 | 21137432 | G | A | intron_variant | MODIFIER | c.1399+283G>A| |
S256 |
| 10 | BAA04g16840 | A04 | 21139092 | C | T | missense_variant | MODERATE | c.1516C>T|p.Arg506Cys |
S46 |