| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g19810 | A02 | 10356776 | G | A | downstream_gene_variant | MODIFIER | c.*4614C>T| |
S122 |
| 2 | BAA02g19810 | A02 | 10357190 | C | T | downstream_gene_variant | MODIFIER | c.*4200G>A| |
S54 |
| 3 | BAA02g19810 | A02 | 10357760 | G | A | downstream_gene_variant | MODIFIER | c.*3630C>T| |
S92 |
| 4 | BAA02g19810 | A02 | 10357875 | C | T | downstream_gene_variant | MODIFIER | c.*3515G>A| |
S226 |
| 5 | BAA02g19810 | A02 | 10358151 | G | A | downstream_gene_variant | MODIFIER | c.*3239C>T| |
S116 |
| 6 | BAA02g19810 | A02 | 10360241 | C | T | downstream_gene_variant | MODIFIER | c.*1149G>A| |
S233 |
| 7 | BAA02g19810 | A02 | 10360316 | C | T | downstream_gene_variant | MODIFIER | c.*1074G>A| |
S152 |
| 8 | BAA02g19810 | A02 | 10360927 | C | T | downstream_gene_variant | MODIFIER | c.*463G>A| |
S189 |
| 9 | BAA02g19810 | A02 | 10361473 | C | T | missense_variant | MODERATE | c.850G>A|p.Glu284Lys |
S180 |
| 10 | BAA02g19810 | A02 | 10361575 | C | T | missense_variant | MODERATE | c.748G>A|p.Asp250Asn |
S267 |
| 11 | BAA02g19810 | A02 | 10361857 | C | T | missense_variant | MODERATE | c.466G>A|p.Val156Ile |
S270 |
| 12 | BAA02g19810 | A02 | 10362627 | G | A | upstream_gene_variant | MODIFIER | c.-305C>T| |
S288 |
| 13 | BAA02g19810 | A02 | 10363094 | C | T | upstream_gene_variant | MODIFIER | c.-772G>A| |
S166 |
| 14 | BAA02g19810 | A02 | 10363303 | G | A | upstream_gene_variant | MODIFIER | c.-981C>T| |
S193 |
| 15 | BAA02g19810 | A02 | 10365852 | G | A | upstream_gene_variant | MODIFIER | c.-3530C>T| |
S41 |
| 16 | BAA02g19810 | A02 | 10366082 | C | T | upstream_gene_variant | MODIFIER | c.-3760G>A| |
S202 |
| 17 | BAA02g19810 | A02 | 10366227 | C | T | upstream_gene_variant | MODIFIER | c.-3905G>A| |
S271 |
| 18 | BAA02g19810 | A02 | 10366309 | C | T | upstream_gene_variant | MODIFIER | c.-3987G>A| |
S183 S198 |
| 19 | BAA02g19810 | A02 | 10366626 | A | C | upstream_gene_variant | MODIFIER | c.-4304T>G| |
S98 |