| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 185151 | BAA02g22940 | A02 | 12463086 | A | T | upstream_gene_variant | MODIFIER | c.-1859A>T| |
S235 |
| 185152 | BAA02g22940 | A02 | 12463509 | G | A | upstream_gene_variant | MODIFIER | c.-1436G>A| |
S143 |
| 185153 | BAA02g22940 | A02 | 12464017 | G | A | upstream_gene_variant | MODIFIER | c.-928G>A| |
S133 |
| 185154 | BAA02g22940 | A02 | 12464590 | G | A | upstream_gene_variant | MODIFIER | c.-355G>A| |
S72 S78 |
| 185155 | BAA02g22940 | A02 | 12465461 | G | A | missense_variant | MODERATE | c.517G>A|p.Glu173Lys |
S109 |
| 185156 | BAA02g22940 | A02 | 12466124 | G | A | missense_variant | MODERATE | c.1180G>A|p.Asp394Asn |
S229 |
| 185157 | BAA02g22940 | A02 | 12466503 | G | A | missense_variant | MODERATE | c.1559G>A|p.Arg520Lys |
S81 S85 |
| 185158 | BAA02g22940 | A02 | 12467090 | C | T | missense_variant | MODERATE | c.1991C>T|p.Thr664Ile |
S32 |
| 185159 | BAA02g22940 | A02 | 12467192 | C | T | missense_variant | MODERATE | c.2093C>T|p.Thr698Ile |
S2 S4 S6 |
| 185160 | BAA02g22940 | A02 | 12467275 | G | A | missense_variant | MODERATE | c.2176G>A|p.Ala726Thr |
S294 |
| 185161 | BAA02g22940 | A02 | 12469876 | G | A | downstream_gene_variant | MODIFIER | c.*691G>A| |
S286 |
| 185162 | BAA02g22940 | A02 | 12470623 | C | T | downstream_gene_variant | MODIFIER | c.*1438C>T| |
S87 |
| 185163 | BAA02g22950 | A02 | 12471836 | G | A | upstream_gene_variant | MODIFIER | c.-4319G>A| |
S143 |
| 185164 | BAA02g22950 | A02 | 12473026 | C | T | upstream_gene_variant | MODIFIER | c.-3129C>T| |
S97 |
| 185165 | BAA02g22950 | A02 | 12473113 | G | A | upstream_gene_variant | MODIFIER | c.-3042G>A| |
S92 |
| 185166 | BAA02g22950 | A02 | 12473203 | C | T | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S183 S198 S255 |
| 185167 | BAA02g22950 | A02 | 12473277 | G | A | upstream_gene_variant | MODIFIER | c.-2878G>A| |
S69 |
| 185168 | BAA02g22950 | A02 | 12473670 | C | T | upstream_gene_variant | MODIFIER | c.-2485C>T| |
S116 |
| 185169 | BAA02g22950 | A02 | 12474656 | G | A | upstream_gene_variant | MODIFIER | c.-1499G>A| |
S150 |
| 185170 | BAA02g22950 | A02 | 12474714 | C | T | upstream_gene_variant | MODIFIER | c.-1441C>T| |
S32 |
| 185171 | BAA02g22950 | A02 | 12475114 | G | A | upstream_gene_variant | MODIFIER | c.-1041G>A| |
S35 |
| 185172 | BAA02g22950 | A02 | 12476065 | C | T | upstream_gene_variant | MODIFIER | c.-90C>T| |
S242 |
| 185173 | BAA02g22950 | A02 | 12477389 | G | A | missense_variant | MODERATE | c.256G>A|p.Gly86Arg |
S4 |
| 185174 | BAA02g22960 | A02 | 12477887 | G | A | downstream_gene_variant | MODIFIER | c.*2999C>T| |
S57 |
| 185175 | BAA02g22960 | A02 | 12478172 | G | A | downstream_gene_variant | MODIFIER | c.*2714C>T| |
S133 |