| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156951 | BAA02g04800 | A02 | 2089437 | C | T | missense_variant | MODERATE | c.4598C>T|p.Ser1533Phe |
S240 |
| 156952 | BAA02g04800 | A02 | 2089917 | C | T | downstream_gene_variant | MODIFIER | c.*464C>T| |
S153 |
| 156953 | BAA02g04800 | A02 | 2090423 | C | T | downstream_gene_variant | MODIFIER | c.*970C>T| |
S18 |
| 156954 | BAA02g04810 | A02 | 2093043 | C | T | synonymous_variant | LOW | c.435G>A|p.Leu145Leu |
S243 S299 |
| 156955 | BAA02g04810 | A02 | 2094306 | G | A | upstream_gene_variant | MODIFIER | c.-370C>T| |
S207 |
| 156956 | BAA02g04810 | A02 | 2094447 | C | T | upstream_gene_variant | MODIFIER | c.-511G>A| |
S77 S82 |
| 156957 | BAA02g04810 | A02 | 2094929 | C | T | upstream_gene_variant | MODIFIER | c.-993G>A| |
S226 |
| 156958 | BAA02g04820 | A02 | 2096632 | C | T | missense_variant | MODERATE | c.697G>A|p.Gly233Ser |
S135 |
| 156959 | BAA02g04820 | A02 | 2097223 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.316-1G>A| |
S65 |
| 156960 | BAA02g04820 | A02 | 2097343 | C | T | missense_variant | MODERATE | c.283G>A|p.Val95Ile |
S277 |
| 156961 | BAA02g04810 | A02 | 2098237 | G | T | upstream_gene_variant | MODIFIER | c.-4301C>A| |
S17 S218 S267 S268 S269 |
| 156962 | BAA02g04810 | A02 | 2098289 | C | T | upstream_gene_variant | MODIFIER | c.-4353G>A| |
S263 |
| 156963 | BAA02g04810 | A02 | 2098398 | C | T | upstream_gene_variant | MODIFIER | c.-4462G>A| |
S103 |
| 156964 | BAA02g04810 | A02 | 2098720 | C | T | upstream_gene_variant | MODIFIER | c.-4784G>A| |
S58 |
| 156965 | BAA02g04820 | A02 | 2098987 | G | A | upstream_gene_variant | MODIFIER | c.-1280C>T| |
S50 |
| 156966 | BAA02g04820 | A02 | 2100267 | G | A | upstream_gene_variant | MODIFIER | c.-2560C>T| |
S223 |
| 156967 | BAA02g04820 | A02 | 2100401 | G | A | upstream_gene_variant | MODIFIER | c.-2694C>T| |
S139 |
| 156968 | BAA02g04820 | A02 | 2100469 | G | A | upstream_gene_variant | MODIFIER | c.-2762C>T| |
S122 |
| 156969 | BAA02g04830 | A02 | 2100757 | G | A | synonymous_variant | LOW | c.117G>A|p.Gly39Gly |
S95 |
| 156970 | BAA02g04830 | A02 | 2100795 | G | A | missense_variant | MODERATE | c.155G>A|p.Gly52Glu |
S34 |
| 156971 | BAA02g04820 | A02 | 2101694 | G | A | upstream_gene_variant | MODIFIER | c.-3987C>T| |
S148 S210 S30 S31 |
| 156972 | BAA02g04820 | A02 | 2101805 | G | A | upstream_gene_variant | MODIFIER | c.-4098C>T| |
S208 S219 |
| 156973 | BAA02g04820 | A02 | 2101816 | C | T | upstream_gene_variant | MODIFIER | c.-4109G>A| |
S279 |
| 156974 | BAA02g04820 | A02 | 2101844 | C | T | upstream_gene_variant | MODIFIER | c.-4137G>A| |
S55 |
| 156975 | BAA02g04820 | A02 | 2102303 | G | A | upstream_gene_variant | MODIFIER | c.-4596C>T| |
S146 |