| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 162001 | BAA02g08990 | A02 | 3968088 | A | C | upstream_gene_variant | MODIFIER | c.-2677A>C| |
S308 |
| 162002 | BAA02g08990 | A02 | 3968707 | C | T | upstream_gene_variant | MODIFIER | c.-2058C>T| |
S278 |
| 162003 | BAA02g08990 | A02 | 3969063 | G | A | upstream_gene_variant | MODIFIER | c.-1702G>A| |
S261 |
| 162004 | BAA02g08990 | A02 | 3969378 | C | T | upstream_gene_variant | MODIFIER | c.-1387C>T| |
S77 S82 |
| 162005 | BAA02g08990 | A02 | 3969402 | C | T | upstream_gene_variant | MODIFIER | c.-1363C>T| |
S62 |
| 162006 | BAA02g08990 | A02 | 3971274 | C | T | synonymous_variant | LOW | c.510C>T|p.Asn170Asn |
S202 |
| 162007 | BAA02g08990 | A02 | 3971960 | G | A | missense_variant | MODERATE | c.1196G>A|p.Gly399Asp |
S184 |
| 162008 | BAA02g08990 | A02 | 3972431 | G | A | downstream_gene_variant | MODIFIER | c.*140G>A| |
S34 |
| 162009 | BAA02g08990 | A02 | 3973094 | G | A | downstream_gene_variant | MODIFIER | c.*803G>A| |
S295 |
| 162010 | BAA02g08990 | A02 | 3973817 | C | T | downstream_gene_variant | MODIFIER | c.*1526C>T| |
S121 |
| 162011 | BAA02g08990 | A02 | 3974727 | C | T | downstream_gene_variant | MODIFIER | c.*2436C>T| |
S136 |
| 162012 | BAA02g08990 | A02 | 3974924 | C | T | downstream_gene_variant | MODIFIER | c.*2633C>T| |
S138 |
| 162013 | BAA02g08990 | A02 | 3975418 | C | T | downstream_gene_variant | MODIFIER | c.*3127C>T| |
S1 S90 |
| 162014 | BAA02g08990 | A02 | 3975640 | G | A | downstream_gene_variant | MODIFIER | c.*3349G>A| |
S133 |
| 162015 | BAA02g08990 | A02 | 3975777 | G | A | downstream_gene_variant | MODIFIER | c.*3486G>A| |
S287 S68 |
| 162016 | BAA02g09000 | A02 | 3983138 | G | A | upstream_gene_variant | MODIFIER | c.-2532G>A| |
S62 |
| 162017 | BAA02g09010 | A02 | 3986526 | G | A | upstream_gene_variant | MODIFIER | c.-2524G>A| |
S107 |
| 162018 | BAA02g09000 | A02 | 3987181 | G | A | missense_variant | MODERATE | c.625G>A|p.Asp209Asn |
S61 |
| 162019 | BAA02g09000 | A02 | 3987223 | G | A | missense_variant | MODERATE | c.667G>A|p.Asp223Asn |
S295 |
| 162020 | BAA02g09000 | A02 | 3987276 | G | A | synonymous_variant | LOW | c.720G>A|p.Glu240Glu |
S298 |
| 162021 | BAA02g09000 | A02 | 3987621 | G | A | missense_variant | MODERATE | c.824G>A|p.Gly275Asp |
S36 |
| 162022 | BAA02g09010 | A02 | 3988560 | C | T | upstream_gene_variant | MODIFIER | c.-490C>T| |
S40 S49 |
| 162023 | BAA02g09010 | A02 | 3988603 | G | A | upstream_gene_variant | MODIFIER | c.-447G>A| |
S187 |
| 162024 | BAA02g09020 | A02 | 3989892 | G | A | synonymous_variant | LOW | c.859C>T|p.Leu287Leu |
S82 S92 |
| 162025 | BAA02g09020 | A02 | 3990077 | G | A | missense_variant | MODERATE | c.767C>T|p.Thr256Ile |
S232 |