| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 83151 | BAA01g44080 | A01 | 29250752 | C | T | splice_region_variant&intron_variant | LOW | c.881-6C>T| |
S183 S198 |
| 83152 | BAA01g44090 | A01 | 29252289 | C | T | missense_variant | MODERATE | c.76C>T|p.Pro26Ser |
S210 S225 |
| 83153 | BAA01g44090 | A01 | 29252777 | C | T | synonymous_variant | LOW | c.564C>T|p.Ser188Ser |
S263 |
| 83154 | BAA01g44090 | A01 | 29252881 | G | A | missense_variant | MODERATE | c.599G>A|p.Gly200Glu |
S284 |
| 83155 | BAA01g44090 | A01 | 29253461 | G | A | stop_gained | HIGH | c.912G>A|p.Trp304* |
S152 |
| 83156 | BAA01g44070 | A01 | 29253707 | C | T | upstream_gene_variant | MODIFIER | c.-4800G>A| |
S11 |
| 83157 | BAA01g44090 | A01 | 29254001 | C | T | synonymous_variant | LOW | c.1221C>T|p.Phe407Phe |
S184 |
| 83158 | BAA01g44080 | A01 | 29255512 | C | T | downstream_gene_variant | MODIFIER | c.*4130C>T| |
S7 |
| 83159 | BAA01g44100 | A01 | 29256128 | C | T | missense_variant | MODERATE | c.932G>A|p.Arg311Lys |
S213 |
| 83160 | BAA01g44100 | A01 | 29256137 | C | T | missense_variant | MODERATE | c.923G>A|p.Ser308Asn |
S148 S210 S30 S31 |
| 83161 | BAA01g44100 | A01 | 29256568 | C | T | synonymous_variant | LOW | c.492G>A|p.Lys164Lys |
S263 |
| 83162 | BAA01g44100 | A01 | 29256665 | C | T | stop_gained | HIGH | c.395G>A|p.Trp132* |
S210 |
| 83163 | BAA01g44100 | A01 | 29257470 | C | T | upstream_gene_variant | MODIFIER | c.-411G>A| |
S97 |
| 83164 | BAA01g44100 | A01 | 29257513 | G | A | upstream_gene_variant | MODIFIER | c.-454C>T| |
S176 |
| 83165 | BAA01g44100 | A01 | 29258118 | G | A | upstream_gene_variant | MODIFIER | c.-1059C>T| |
S212 |
| 83166 | BAA01g44100 | A01 | 29258826 | G | A | upstream_gene_variant | MODIFIER | c.-1767C>T| |
S245 |
| 83167 | BAA01g44100 | A01 | 29258950 | G | A | upstream_gene_variant | MODIFIER | c.-1891C>T| |
S139 |
| 83168 | BAA01g44100 | A01 | 29260231 | A | T | upstream_gene_variant | MODIFIER | c.-3172T>A| |
S204 |
| 83169 | BAA01g44100 | A01 | 29260608 | C | T | upstream_gene_variant | MODIFIER | c.-3549G>A| |
S275 |
| 83170 | BAA01g44100 | A01 | 29261365 | C | T | upstream_gene_variant | MODIFIER | c.-4306G>A| |
S12 |
| 83171 | BAA01g44100 | A01 | 29261366 | C | T | upstream_gene_variant | MODIFIER | c.-4307G>A| |
S166 S92 |
| 83172 | BAA01g44100 | A01 | 29261793 | G | A | upstream_gene_variant | MODIFIER | c.-4734C>T| |
S117 |
| 83173 | BAA01g44110 | A01 | 29262380 | C | A | downstream_gene_variant | MODIFIER | c.*495G>T| |
S80 |
| 83174 | BAA01g44110 | A01 | 29263327 | C | T | missense_variant | MODERATE | c.1981G>A|p.Gly661Arg |
S256 |
| 83175 | BAA01g44110 | A01 | 29264850 | C | T | missense_variant | MODERATE | c.916G>A|p.Gly306Arg |
S264 |