| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 197251 | BAA02g29230 | A02 | 16709103 | G | A | missense_variant | MODERATE | c.554C>T|p.Ser185Phe |
S113 |
| 197252 | BAA02g29230 | A02 | 16709114 | C | T | synonymous_variant | LOW | c.543G>A|p.Arg181Arg |
S167 |
| 197253 | BAA02g29240 | A02 | 16709998 | G | A | upstream_gene_variant | MODIFIER | c.-1567G>A| |
S134 |
| 197254 | BAA02g29240 | A02 | 16710018 | C | T | upstream_gene_variant | MODIFIER | c.-1547C>T| |
S216 |
| 197255 | BAA02g29240 | A02 | 16710201 | C | T | upstream_gene_variant | MODIFIER | c.-1364C>T| |
S286 |
| 197256 | BAA02g29230 | A02 | 16710631 | C | T | upstream_gene_variant | MODIFIER | c.-51G>A| |
S159 S188 S243 S276 S298 S299 |
| 197257 | BAA02g29230 | A02 | 16710646 | C | T | upstream_gene_variant | MODIFIER | c.-66G>A| |
S219 S72 |
| 197258 | BAA02g29230 | A02 | 16710715 | C | T | upstream_gene_variant | MODIFIER | c.-135G>A| |
S218 |
| 197259 | BAA02g29230 | A02 | 16710895 | C | T | upstream_gene_variant | MODIFIER | c.-315G>A| |
S303 |
| 197260 | BAA02g29230 | A02 | 16711400 | C | T | upstream_gene_variant | MODIFIER | c.-820G>A| |
S15 |
| 197261 | BAA02g29230 | A02 | 16711447 | G | A | upstream_gene_variant | MODIFIER | c.-867C>T| |
S95 |
| 197262 | BAA02g29230 | A02 | 16711485 | C | T | upstream_gene_variant | MODIFIER | c.-905G>A| |
S240 |
| 197263 | BAA02g29240 | A02 | 16711846 | G | A | synonymous_variant | LOW | c.282G>A|p.Lys94Lys |
S168 |
| 197264 | BAA02g29230 | A02 | 16712198 | C | T | upstream_gene_variant | MODIFIER | c.-1618G>A| |
S202 |
| 197265 | BAA02g29240 | A02 | 16712284 | G | A | missense_variant | MODERATE | c.557G>A|p.Arg186Lys |
S190 |
| 197266 | BAA02g29240 | A02 | 16712375 | G | A | synonymous_variant | LOW | c.648G>A|p.Lys216Lys |
S159 S243 |
| 197267 | BAA02g29240 | A02 | 16714192 | G | A | missense_variant | MODERATE | c.1480G>A|p.Gly494Arg |
S191 |
| 197268 | BAA02g29230 | A02 | 16714895 | G | A | upstream_gene_variant | MODIFIER | c.-4315C>T| |
S224 |
| 197269 | BAA02g29250 | A02 | 16717013 | C | T | missense_variant | MODERATE | c.631C>T|p.Leu211Phe |
S65 |
| 197270 | BAA02g29250 | A02 | 16717087 | G | A | stop_gained | HIGH | c.705G>A|p.Trp235* |
S210 |
| 197271 | BAA02g29250 | A02 | 16717606 | G | A | splice_region_variant&intron_variant | LOW | c.1128+5G>A| |
S302 |
| 197272 | BAA02g29250 | A02 | 16718192 | C | T | synonymous_variant | LOW | c.1539C>T|p.Asn513Asn |
S122 |
| 197273 | BAA02g29240 | A02 | 16718761 | G | A | downstream_gene_variant | MODIFIER | c.*3953G>A| |
S34 |
| 197274 | BAA02g29250 | A02 | 16719169 | G | A | missense_variant | MODERATE | c.2212G>A|p.Glu738Lys |
S291 |
| 197275 | BAA02g29250 | A02 | 16720324 | C | T | downstream_gene_variant | MODIFIER | c.*615C>T| |
S135 S266 |