| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 34151 | BAA01g23060 | A01 | 11780574 | G | A | synonymous_variant | LOW | c.72C>T|p.His24His |
S278 |
| 34152 | BAA01g23050 | A01 | 11780642 | G | A | downstream_gene_variant | MODIFIER | c.*2339G>A| |
S246 |
| 34153 | BAA01g23060 | A01 | 11780706 | C | T | missense_variant | MODERATE | c.23G>A|p.Arg8Lys |
S136 S186 S275 S301 S304 |
| 34154 | BAA01g23060 | A01 | 11781564 | G | A | upstream_gene_variant | MODIFIER | c.-836C>T| |
S105 S106 |
| 34155 | BAA01g23060 | A01 | 11781920 | G | A | upstream_gene_variant | MODIFIER | c.-1192C>T| |
S239 |
| 34156 | BAA01g23060 | A01 | 11783346 | C | T | upstream_gene_variant | MODIFIER | c.-2618G>A| |
S286 |
| 34157 | BAA01g23060 | A01 | 11783956 | G | A | upstream_gene_variant | MODIFIER | c.-3228C>T| |
S149 |
| 34158 | BAA01g23060 | A01 | 11785274 | C | T | upstream_gene_variant | MODIFIER | c.-4546G>A| |
S54 |
| 34159 | BAA01g23070 | A01 | 11787087 | C | T | downstream_gene_variant | MODIFIER | c.*4063G>A| |
S36 |
| 34160 | BAA01g23070 | A01 | 11787287 | C | T | downstream_gene_variant | MODIFIER | c.*3863G>A| |
S267 |
| 34161 | BAA01g23070 | A01 | 11787359 | G | A | downstream_gene_variant | MODIFIER | c.*3791C>T| |
S125 |
| 34162 | BAA01g23070 | A01 | 11787408 | C | T | downstream_gene_variant | MODIFIER | c.*3742G>A| |
S158 |
| 34163 | BAA01g23070 | A01 | 11787591 | C | T | downstream_gene_variant | MODIFIER | c.*3559G>A| |
S7 |
| 34164 | BAA01g23070 | A01 | 11788292 | A | T | downstream_gene_variant | MODIFIER | c.*2858T>A| |
S194 |
| 34165 | BAA01g23070 | A01 | 11788649 | G | A | downstream_gene_variant | MODIFIER | c.*2501C>T| |
S32 |
| 34166 | BAA01g23070 | A01 | 11788744 | C | T | downstream_gene_variant | MODIFIER | c.*2406G>A| |
S47 |
| 34167 | BAA01g23080 | A01 | 11790972 | C | T | upstream_gene_variant | MODIFIER | c.-3661C>T| |
S261 |
| 34168 | BAA01g23080 | A01 | 11791144 | G | A | upstream_gene_variant | MODIFIER | c.-3489G>A| |
S96 |
| 34169 | BAA01g23070 | A01 | 11791224 | C | T | missense_variant | MODERATE | c.2236G>A|p.Glu746Lys |
S266 |
| 34170 | BAA01g23070 | A01 | 11791386 | C | T | synonymous_variant | LOW | c.2148G>A|p.Ser716Ser |
S198 |
| 34171 | BAA01g23070 | A01 | 11791439 | G | A | missense_variant | MODERATE | c.2095C>T|p.Leu699Phe |
S13 S144 |
| 34172 | BAA01g23070 | A01 | 11791682 | G | A | stop_gained | HIGH | c.1951C>T|p.Gln651* |
S142 |
| 34173 | BAA01g23070 | A01 | 11793619 | G | A | stop_gained | HIGH | c.94C>T|p.Gln32* |
S262 |
| 34174 | BAA01g23070 | A01 | 11793882 | G | A | upstream_gene_variant | MODIFIER | c.-170C>T| |
S226 |
| 34175 | BAA01g23070 | A01 | 11794068 | G | A | upstream_gene_variant | MODIFIER | c.-356C>T| |
S246 |