| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 167101 | BAA02g13000 | A02 | 5813250 | C | T | upstream_gene_variant | MODIFIER | c.-2278G>A| |
S178 |
| 167102 | BAA02g13000 | A02 | 5813252 | C | T | upstream_gene_variant | MODIFIER | c.-2280G>A| |
S107 |
| 167103 | BAA02g13000 | A02 | 5813350 | G | A | upstream_gene_variant | MODIFIER | c.-2378C>T| |
S134 |
| 167104 | BAA02g13000 | A02 | 5813942 | G | A | upstream_gene_variant | MODIFIER | c.-2970C>T| |
S136 |
| 167105 | BAA02g13000 | A02 | 5813996 | G | A | upstream_gene_variant | MODIFIER | c.-3024C>T| |
S69 |
| 167106 | BAA02g13020 | A02 | 5816576 | G | A | upstream_gene_variant | MODIFIER | c.-3084G>A| |
S56 |
| 167107 | BAA02g13020 | A02 | 5819749 | G | A | synonymous_variant | LOW | c.90G>A|p.Thr30Thr |
S123 |
| 167108 | BAA02g13020 | A02 | 5820199 | G | A | synonymous_variant | LOW | c.540G>A|p.Lys180Lys |
S176 |
| 167109 | BAA02g13020 | A02 | 5820416 | C | T | missense_variant | MODERATE | c.757C>T|p.Pro253Ser |
S272 |
| 167110 | BAA02g13020 | A02 | 5821125 | G | A | missense_variant | MODERATE | c.1214G>A|p.Gly405Glu |
S168 |
| 167111 | BAA02g13030 | A02 | 5821513 | C | T | downstream_gene_variant | MODIFIER | c.*3283G>A| |
S270 |
| 167112 | BAA02g13030 | A02 | 5822197 | G | A | downstream_gene_variant | MODIFIER | c.*2599C>T| |
S98 |
| 167113 | BAA02g13030 | A02 | 5822286 | C | T | downstream_gene_variant | MODIFIER | c.*2510G>A| |
S212 |
| 167114 | BAA02g13030 | A02 | 5822477 | G | A | downstream_gene_variant | MODIFIER | c.*2319C>T| |
S260 |
| 167115 | BAA02g13030 | A02 | 5822974 | C | T | downstream_gene_variant | MODIFIER | c.*1822G>A| |
S299 |
| 167116 | BAA02g13030 | A02 | 5823214 | G | A | downstream_gene_variant | MODIFIER | c.*1582C>T| |
S282 |
| 167117 | BAA02g13030 | A02 | 5823311 | C | T | downstream_gene_variant | MODIFIER | c.*1485G>A| |
S32 |
| 167118 | BAA02g13030 | A02 | 5823483 | C | T | downstream_gene_variant | MODIFIER | c.*1313G>A| |
S277 |
| 167119 | BAA02g13020 | A02 | 5823668 | C | T | missense_variant | MODERATE | c.1819C>T|p.Pro607Ser |
S130 |
| 167120 | BAA02g13020 | A02 | 5825768 | G | A | downstream_gene_variant | MODIFIER | c.*1444G>A| |
S256 |
| 167121 | BAA02g13030 | A02 | 5829644 | C | T | upstream_gene_variant | MODIFIER | c.-2601G>A| |
S283 |
| 167122 | BAA02g13030 | A02 | 5830291 | G | A | upstream_gene_variant | MODIFIER | c.-3248C>T| |
S10 |
| 167123 | BAA02g13030 | A02 | 5831261 | C | T | upstream_gene_variant | MODIFIER | c.-4218G>A| |
S153 |
| 167124 | BAA02g13030 | A02 | 5831335 | C | T | upstream_gene_variant | MODIFIER | c.-4292G>A| |
S79 S91 |
| 167125 | BAA02g13030 | A02 | 5831423 | G | A | upstream_gene_variant | MODIFIER | c.-4380C>T| |
S155 S211 |