| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g26100 | A10 | 20809278 | G | A | downstream_gene_variant | MODIFIER | c.*1229C>T| |
S57 |
| 2 | BAA10g26100 | A10 | 20810959 | C | T | missense_variant | MODERATE | c.1945G>A|p.Val649Ile |
S23 |
| 3 | BAA10g26100 | A10 | 20811372 | C | T | missense_variant | MODERATE | c.1532G>A|p.Arg511Lys |
S224 |
| 4 | BAA10g26100 | A10 | 20811998 | C | T | synonymous_variant | LOW | c.906G>A|p.Gly302Gly |
S244 |
| 5 | BAA10g26100 | A10 | 20814400 | T | A | upstream_gene_variant | MODIFIER | c.-1497A>T| |
S157 S163 |
| 6 | BAA10g26100 | A10 | 20815371 | G | A | upstream_gene_variant | MODIFIER | c.-2468C>T| |
S17 |
| 7 | BAA10g26100 | A10 | 20816177 | G | A | upstream_gene_variant | MODIFIER | c.-3274C>T| |
S138 |
| 8 | BAA10g26100 | A10 | 20816195 | C | T | upstream_gene_variant | MODIFIER | c.-3292G>A| |
S268 |