| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g27980 | A09 | 18376169 | C | T | missense_variant | MODERATE | c.1310G>A|p.Arg437Lys |
S268 |
| 2 | BAA09g27980 | A09 | 18376377 | C | T | missense_variant | MODERATE | c.1102G>A|p.Gly368Arg |
S277 |
| 3 | BAA09g27980 | A09 | 18378656 | C | T | upstream_gene_variant | MODIFIER | c.-1093G>A| |
S206 S26 |
| 4 | BAA09g27980 | A09 | 18378904 | C | T | upstream_gene_variant | MODIFIER | c.-1341G>A| |
S306 |
| 5 | BAA09g27980 | A09 | 18379918 | C | T | upstream_gene_variant | MODIFIER | c.-2355G>A| |
S272 |
| 6 | BAA09g27980 | A09 | 18380419 | C | T | upstream_gene_variant | MODIFIER | c.-2856G>A| |
S14 |
| 7 | BAA09g27980 | A09 | 18381160 | C | T | upstream_gene_variant | MODIFIER | c.-3597G>A| |
S109 |
| 8 | BAA09g27980 | A09 | 18382544 | G | A | upstream_gene_variant | MODIFIER | c.-4981C>T| |
S152 |