| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g56160 | A09 | 55954151 | G | A | missense_variant | MODERATE | c.1528C>T|p.Leu510Phe |
S244 |
| 2 | BAA09g56160 | A09 | 55954169 | G | A | missense_variant | MODERATE | c.1510C>T|p.Pro504Ser |
S57 |
| 3 | BAA09g56160 | A09 | 55958621 | G | A | intron_variant | MODIFIER | c.269-865C>T| |
S13 |
| 4 | BAA09g56160 | A09 | 55958885 | C | T | intron_variant | MODIFIER | c.269-1129G>A| |
S41 |
| 5 | BAA09g56160 | A09 | 55961145 | G | A | missense_variant | MODERATE | c.59C>T|p.Ser20Leu |
S295 |
| 6 | BAA09g56160 | A09 | 55961167 | G | A | missense_variant | MODERATE | c.37C>T|p.Leu13Phe |
S263 |
| 7 | BAA09g56160 | A09 | 55962478 | C | T | upstream_gene_variant | MODIFIER | c.-1275G>A| |
S205 |
| 8 | BAA09g56160 | A09 | 55965431 | C | T | upstream_gene_variant | MODIFIER | c.-4228G>A| |
S207 |
| 9 | BAA09g56160 | A09 | 55966018 | C | T | upstream_gene_variant | MODIFIER | c.-4815G>A| |
S78 S83 |
| 10 | BAA09g56160 | A09 | 55966022 | G | A | upstream_gene_variant | MODIFIER | c.-4819C>T| |
S197 |