| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 183151 | BAA02g21870 | A02 | 11774386 | G | A | upstream_gene_variant | MODIFIER | c.-4612G>A| |
S225 |
| 183152 | BAA02g21870 | A02 | 11775041 | C | T | upstream_gene_variant | MODIFIER | c.-3957C>T| |
S301 S304 |
| 183153 | BAA02g21870 | A02 | 11775206 | G | A | upstream_gene_variant | MODIFIER | c.-3792G>A| |
S33 |
| 183154 | BAA02g21870 | A02 | 11775982 | G | A | upstream_gene_variant | MODIFIER | c.-3016G>A| |
S69 |
| 183155 | BAA02g21870 | A02 | 11776073 | C | T | upstream_gene_variant | MODIFIER | c.-2925C>T| |
S183 S198 |
| 183156 | BAA02g21870 | A02 | 11776304 | T | G | upstream_gene_variant | MODIFIER | c.-2694T>G| |
S289 S290 |
| 183157 | BAA02g21860 | A02 | 11777305 | G | A | synonymous_variant | LOW | c.507C>T|p.Leu169Leu |
S192 |
| 183158 | BAA02g21860 | A02 | 11777405 | G | A | missense_variant | MODERATE | c.407C>T|p.Thr136Ile |
S291 |
| 183159 | BAA02g21870 | A02 | 11777648 | C | T | upstream_gene_variant | MODIFIER | c.-1350C>T| |
S96 |
| 183160 | BAA02g21860 | A02 | 11778672 | G | A | upstream_gene_variant | MODIFIER | c.-756C>T| |
S204 |
| 183161 | BAA02g21860 | A02 | 11778817 | G | A | upstream_gene_variant | MODIFIER | c.-901C>T| |
S149 |
| 183162 | BAA02g21860 | A02 | 11778828 | G | A | upstream_gene_variant | MODIFIER | c.-912C>T| |
S126 |
| 183163 | BAA02g21860 | A02 | 11781179 | G | A | upstream_gene_variant | MODIFIER | c.-3263C>T| |
S20 |
| 183164 | BAA02g21860 | A02 | 11782496 | C | T | upstream_gene_variant | MODIFIER | c.-4580G>A| |
S203 |
| 183165 | BAA02g21860 | A02 | 11782603 | C | T | upstream_gene_variant | MODIFIER | c.-4687G>A| |
S296 |
| 183166 | BAA02g21880 | A02 | 11783312 | G | A | upstream_gene_variant | MODIFIER | c.-1604C>T| |
S204 |
| 183167 | BAA02g21880 | A02 | 11784265 | G | A | upstream_gene_variant | MODIFIER | c.-2557C>T| |
S116 |
| 183168 | BAA02g21880 | A02 | 11784348 | G | A | upstream_gene_variant | MODIFIER | c.-2640C>T| |
S126 |
| 183169 | BAA02g21880 | A02 | 11786507 | G | A | upstream_gene_variant | MODIFIER | c.-4799C>T| |
S136 |
| 183170 | BAA02g21880-BAA02g21890 | A02 | 11787813 | G | A | intergenic_region | MODIFIER | n.11787813G>A| |
S256 |
| 183171 | BAA02g21890 | A02 | 11788536 | G | A | downstream_gene_variant | MODIFIER | c.*4750C>T| |
S197 |
| 183172 | BAA02g21890 | A02 | 11788589 | G | A | downstream_gene_variant | MODIFIER | c.*4697C>T| |
S19 |
| 183173 | BAA02g21890 | A02 | 11792120 | G | A | downstream_gene_variant | MODIFIER | c.*1166C>T| |
S37 |
| 183174 | BAA02g21890 | A02 | 11792210 | C | T | downstream_gene_variant | MODIFIER | c.*1076G>A| |
S221 |
| 183175 | BAA02g21890 | A02 | 11792528 | G | A | downstream_gene_variant | MODIFIER | c.*758C>T| |
S235 |