| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 14051 | BAA01g10970 | A01 | 5052981 | C | T | upstream_gene_variant | MODIFIER | c.-2056C>T| |
S246 |
| 14052 | BAA01g10970 | A01 | 5053794 | C | T | upstream_gene_variant | MODIFIER | c.-1243C>T| |
S1 S90 |
| 14053 | BAA01g10970 | A01 | 5054380 | G | A | upstream_gene_variant | MODIFIER | c.-657G>A| |
S173 |
| 14054 | BAA01g10970 | A01 | 5055179 | C | T | missense_variant | MODERATE | c.143C>T|p.Thr48Met |
S119 |
| 14055 | BAA01g10960 | A01 | 5055308 | C | T | downstream_gene_variant | MODIFIER | c.*2739C>T| |
S79 S84 |
| 14056 | BAA01g10960 | A01 | 5055322 | G | A | downstream_gene_variant | MODIFIER | c.*2753G>A| |
S146 |
| 14057 | BAA01g10970 | A01 | 5058224 | G | A | downstream_gene_variant | MODIFIER | c.*2951G>A| |
S293 |
| 14058 | BAA01g10970 | A01 | 5058707 | G | A | downstream_gene_variant | MODIFIER | c.*3434G>A| |
S133 |
| 14059 | BAA01g10970 | A01 | 5059678 | C | T | downstream_gene_variant | MODIFIER | c.*4405C>T| |
S20 |
| 14060 | BAA01g10970 | A01 | 5060176 | G | A | downstream_gene_variant | MODIFIER | c.*4903G>A| |
S153 |
| 14061 | BAA01g10980 | A01 | 5061107 | C | T | downstream_gene_variant | MODIFIER | c.*4795G>A| |
S107 |
| 14062 | BAA01g10980 | A01 | 5061560 | G | A | downstream_gene_variant | MODIFIER | c.*4342C>T| |
S229 |
| 14063 | BAA01g10990 | A01 | 5062005 | G | A | upstream_gene_variant | MODIFIER | c.-4913G>A| |
S153 |
| 14064 | BAA01g10990 | A01 | 5063925 | G | A | upstream_gene_variant | MODIFIER | c.-2993G>A| |
S103 |
| 14065 | BAA01g10990 | A01 | 5065115 | G | A | upstream_gene_variant | MODIFIER | c.-1803G>A| |
S279 |
| 14066 | BAA01g10990 | A01 | 5065624 | G | A | upstream_gene_variant | MODIFIER | c.-1294G>A| |
S95 |
| 14067 | BAA01g10980 | A01 | 5066114 | G | A | missense_variant | MODERATE | c.154C>T|p.Pro52Ser |
S177 |
| 14068 | BAA01g10980 | A01 | 5066167 | G | A | missense_variant | MODERATE | c.101C>T|p.Pro34Leu |
S149 |
| 14069 | BAA01g10980 | A01 | 5066642 | C | T | upstream_gene_variant | MODIFIER | c.-375G>A| |
S184 |
| 14070 | BAA01g10980 | A01 | 5068142 | C | T | upstream_gene_variant | MODIFIER | c.-1875G>A| |
S275 |
| 14071 | BAA01g11000 | A01 | 5071434 | G | A | missense_variant | MODERATE | c.1237C>T|p.Pro413Ser |
S121 |
| 14072 | BAA01g11000 | A01 | 5072104 | G | A | synonymous_variant | LOW | c.567C>T|p.Phe189Phe |
S133 |
| 14073 | BAA01g11000 | A01 | 5073424 | G | A | upstream_gene_variant | MODIFIER | c.-754C>T| |
S122 |
| 14074 | BAA01g11000 | A01 | 5074705 | G | A | upstream_gene_variant | MODIFIER | c.-2035C>T| |
S306 S308 |
| 14075 | BAA01g11000 | A01 | 5075323 | G | A | upstream_gene_variant | MODIFIER | c.-2653C>T| |
S298 |