| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 193401 | BAA02g27370 | A02 | 15389551 | G | A | upstream_gene_variant | MODIFIER | c.-2289C>T| |
S259 |
| 193402 | BAA02g27370 | A02 | 15390945 | C | T | upstream_gene_variant | MODIFIER | c.-3683G>A| |
S120 |
| 193403 | BAA02g27370 | A02 | 15391044 | G | A | upstream_gene_variant | MODIFIER | c.-3782C>T| |
S208 |
| 193404 | BAA02g27370 | A02 | 15391398 | C | T | upstream_gene_variant | MODIFIER | c.-4136G>A| |
S296 |
| 193405 | BAA02g27380 | A02 | 15392382 | G | A | missense_variant | MODERATE | c.377G>A|p.Ser126Asn |
S188 |
| 193406 | BAA02g27380 | A02 | 15392788 | G | A | missense_variant | MODERATE | c.563G>A|p.Arg188Lys |
S173 |
| 193407 | BAA02g27380 | A02 | 15393179 | G | A | downstream_gene_variant | MODIFIER | c.*345G>A| |
S249 |
| 193408 | BAA02g27390 | A02 | 15394822 | G | A | upstream_gene_variant | MODIFIER | c.-3699G>A| |
S245 |
| 193409 | BAA02g27390 | A02 | 15395245 | G | A | upstream_gene_variant | MODIFIER | c.-3276G>A| |
S56 |
| 193410 | BAA02g27390 | A02 | 15395775 | C | T | upstream_gene_variant | MODIFIER | c.-2746C>T| |
S282 |
| 193411 | BAA02g27390 | A02 | 15396675 | G | A | upstream_gene_variant | MODIFIER | c.-1846G>A| |
S45 |
| 193412 | BAA02g27390 | A02 | 15397639 | G | A | upstream_gene_variant | MODIFIER | c.-882G>A| |
S286 |
| 193413 | BAA02g27390 | A02 | 15398724 | C | T | intron_variant | MODIFIER | c.46+158C>T| |
S203 |
| 193414 | BAA02g27390 | A02 | 15399534 | G | A | intron_variant | MODIFIER | c.46+968G>A| |
S92 |
| 193415 | BAA02g27390 | A02 | 15399799 | C | T | intron_variant | MODIFIER | c.47-978C>T| |
S183 S198 |
| 193416 | BAA02g27390 | A02 | 15400952 | C | T | splice_region_variant&intron_variant | LOW | c.214+8C>T| |
S289 S290 |
| 193417 | BAA02g27390 | A02 | 15402336 | C | T | missense_variant | MODERATE | c.1129C>T|p.Leu377Phe |
S221 |
| 193418 | BAA02g27390 | A02 | 15402731 | C | T | intron_variant | MODIFIER | c.1440+84C>T| |
S40 |
| 193419 | BAA02g27390 | A02 | 15403105 | C | T | intron_variant | MODIFIER | c.1441-294C>T| |
S135 |
| 193420 | BAA02g27390 | A02 | 15403148 | G | A | intron_variant | MODIFIER | c.1441-251G>A| |
S136 |
| 193421 | BAA02g27390 | A02 | 15403227 | G | A | intron_variant | MODIFIER | c.1441-172G>A| |
S186 |
| 193422 | BAA02g27390 | A02 | 15403340 | C | T | intron_variant | MODIFIER | c.1441-59C>T| |
S283 |
| 193423 | BAA02g27390 | A02 | 15403360 | G | A | intron_variant | MODIFIER | c.1441-39G>A| |
S149 |
| 193424 | BAA02g27390 | A02 | 15403753 | C | T | stop_gained | HIGH | c.1795C>T|p.Gln599* |
S176 |
| 193425 | BAA02g27390 | A02 | 15403931 | C | T | missense_variant | MODERATE | c.1973C>T|p.Ser658Phe |
S127 |