| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g20160 | A05 | 12298580 | C | T | upstream_gene_variant | MODIFIER | c.-2802C>T| |
S67 |
| 2 | BAA05g20160 | A05 | 12298702 | G | T | upstream_gene_variant | MODIFIER | c.-2680G>T| |
S238 |
| 3 | BAA05g20160 | A05 | 12300184 | C | T | upstream_gene_variant | MODIFIER | c.-1198C>T| |
S71 |
| 4 | BAA05g20160 | A05 | 12300484 | A | C | upstream_gene_variant | MODIFIER | c.-898A>C| |
S111 S113 S131 S133 S139 S161 S17 S174 S2 S209 S223 S36 S8 |
| 5 | BAA05g20160 | A05 | 12300606 | G | A | upstream_gene_variant | MODIFIER | c.-776G>A| |
S3 |
| 6 | BAA05g20160 | A05 | 12301643 | C | T | missense_variant | MODERATE | c.262C>T|p.Pro88Ser |
S58 |
| 7 | BAA05g20160 | A05 | 12302276 | G | A | missense_variant | MODERATE | c.895G>A|p.Glu299Lys |
S3 |
| 8 | BAA05g20160 | A05 | 12302619 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1095-1G>A| |
S192 |
| 9 | BAA05g20160 | A05 | 12302721 | G | A | missense_variant | MODERATE | c.1196G>A|p.Gly399Asp |
S294 |
| 10 | BAA05g20160 | A05 | 12303043 | A | C | synonymous_variant | LOW | c.1518A>C|p.Thr506Thr |
S218 S267 |
| 11 | BAA05g20160 | A05 | 12303352 | T | G | downstream_gene_variant | MODIFIER | c.*156T>G| |
S295 |
| 12 | BAA05g20160 | A05 | 12304583 | G | T | downstream_gene_variant | MODIFIER | c.*1387G>T| |
S60 |
| 13 | BAA05g20160 | A05 | 12304832 | G | A | downstream_gene_variant | MODIFIER | c.*1636G>A| |
S11 |
| 14 | BAA05g20160 | A05 | 12305456 | G | A | downstream_gene_variant | MODIFIER | c.*2260G>A| |
S16 |
| 15 | BAA05g20160 | A05 | 12305552 | C | A | downstream_gene_variant | MODIFIER | c.*2356C>A| |
S144 S247 S263 S277 S56 |
| 16 | BAA05g20160 | A05 | 12307177 | G | A | downstream_gene_variant | MODIFIER | c.*3981G>A| |
S238 |
| 17 | BAA05g20160 | A05 | 12307302 | C | T | downstream_gene_variant | MODIFIER | c.*4106C>T| |
S17 |
| 18 | BAA05g20160 | A05 | 12307500 | G | A | downstream_gene_variant | MODIFIER | c.*4304G>A| |
S60 |