| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 174851 | BAA02g17550 | A02 | 8755426 | G | A | upstream_gene_variant | MODIFIER | c.-4451C>T| |
S162 |
| 174852 | BAA02g17550 | A02 | 8755797 | G | A | upstream_gene_variant | MODIFIER | c.-4822C>T| |
S288 S45 |
| 174853 | BAA02g17560 | A02 | 8756222 | G | A | upstream_gene_variant | MODIFIER | c.-747G>A| |
S187 |
| 174854 | BAA02g17560 | A02 | 8756364 | C | T | upstream_gene_variant | MODIFIER | c.-605C>T| |
S75 S81 |
| 174855 | BAA02g17560 | A02 | 8756465 | C | T | upstream_gene_variant | MODIFIER | c.-504C>T| |
S131 |
| 174856 | BAA02g17560 | A02 | 8756480 | G | A | upstream_gene_variant | MODIFIER | c.-489G>A| |
S297 |
| 174857 | BAA02g17560 | A02 | 8756703 | C | T | upstream_gene_variant | MODIFIER | c.-266C>T| |
S216 |
| 174858 | BAA02g17560 | A02 | 8756725 | C | T | upstream_gene_variant | MODIFIER | c.-244C>T| |
S16 |
| 174859 | BAA02g17560 | A02 | 8756757 | G | A | upstream_gene_variant | MODIFIER | c.-212G>A| |
S259 |
| 174860 | BAA02g17560 | A02 | 8757481 | C | T | missense_variant | MODERATE | c.175C>T|p.Pro59Ser |
S160 |
| 174861 | BAA02g17560 | A02 | 8758300 | C | T | missense_variant | MODERATE | c.899C>T|p.Ala300Val |
S107 |
| 174862 | BAA02g17560 | A02 | 8758655 | G | A | synonymous_variant | LOW | c.1254G>A|p.Glu418Glu |
S197 |
| 174863 | BAA02g17560 | A02 | 8759235 | G | A | missense_variant | MODERATE | c.1834G>A|p.Glu612Lys |
S303 |
| 174864 | BAA02g17560 | A02 | 8759898 | G | A | missense_variant | MODERATE | c.2497G>A|p.Glu833Lys |
S247 |
| 174865 | BAA02g17560 | A02 | 8760696 | G | A | missense_variant | MODERATE | c.3295G>A|p.Asp1099Asn |
S279 |
| 174866 | BAA02g17560 | A02 | 8760820 | G | A | missense_variant | MODERATE | c.3419G>A|p.Ser1140Asn |
S4 |
| 174867 | BAA02g17560 | A02 | 8761061 | G | A | synonymous_variant | LOW | c.3660G>A|p.Lys1220Lys |
S217 S248 |
| 174868 | BAA02g17570 | A02 | 8762173 | G | A | synonymous_variant | LOW | c.747C>T|p.Ile249Ile |
S155 S211 |
| 174869 | BAA02g17570 | A02 | 8763275 | G | A | missense_variant | MODERATE | c.169C>T|p.Pro57Ser |
S64 |
| 174870 | BAA02g17570 | A02 | 8763605 | G | A | upstream_gene_variant | MODIFIER | c.-97C>T| |
S53 |
| 174871 | BAA02g17570 | A02 | 8763827 | G | A | upstream_gene_variant | MODIFIER | c.-319C>T| |
S187 |
| 174872 | BAA02g17570 | A02 | 8764615 | G | A | upstream_gene_variant | MODIFIER | c.-1107C>T| |
S187 |
| 174873 | BAA02g17570 | A02 | 8765019 | C | T | upstream_gene_variant | MODIFIER | c.-1511G>A| |
S87 |
| 174874 | BAA02g17570 | A02 | 8766493 | C | T | upstream_gene_variant | MODIFIER | c.-2985G>A| |
S1 S90 |
| 174875 | BAA02g17580 | A02 | 8766925 | C | T | missense_variant | MODERATE | c.436G>A|p.Val146Met |
S135 |