| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 185901 | BAA02g23430 | A02 | 12770661 | G | A | upstream_gene_variant | MODIFIER | c.-629G>A| |
S279 |
| 185902 | BAA02g23430 | A02 | 12772996 | G | A | missense_variant | MODERATE | c.1004G>A|p.Gly335Glu |
S5 |
| 185903 | BAA02g23430 | A02 | 12774411 | C | T | downstream_gene_variant | MODIFIER | c.*1279C>T| |
S171 |
| 185904 | BAA02g23440 | A02 | 12776436 | G | A | upstream_gene_variant | MODIFIER | c.-4644G>A| |
S13 S140 S168 S279 S64 |
| 185905 | BAA02g23440 | A02 | 12777346 | G | A | upstream_gene_variant | MODIFIER | c.-3734G>A| |
S28 |
| 185906 | BAA02g23440 | A02 | 12777732 | G | T | upstream_gene_variant | MODIFIER | c.-3348G>T| |
S250 |
| 185907 | BAA02g23440 | A02 | 12779353 | G | A | upstream_gene_variant | MODIFIER | c.-1727G>A| |
S64 |
| 185908 | BAA02g23440 | A02 | 12779362 | G | A | upstream_gene_variant | MODIFIER | c.-1718G>A| |
S128 |
| 185909 | BAA02g23440 | A02 | 12780224 | G | A | upstream_gene_variant | MODIFIER | c.-856G>A| |
S255 |
| 185910 | BAA02g23440 | A02 | 12780418 | C | T | upstream_gene_variant | MODIFIER | c.-662C>T| |
S33 |
| 185911 | BAA02g23440 | A02 | 12780436 | G | A | upstream_gene_variant | MODIFIER | c.-644G>A| |
S86 S90 S98 |
| 185912 | BAA02g23450 | A02 | 12782102 | G | A | upstream_gene_variant | MODIFIER | c.-1110G>A| |
S202 |
| 185913 | BAA02g23450 | A02 | 12782110 | C | T | upstream_gene_variant | MODIFIER | c.-1102C>T| |
S185 |
| 185914 | BAA02g23450 | A02 | 12782342 | C | T | upstream_gene_variant | MODIFIER | c.-870C>T| |
S180 |
| 185915 | BAA02g23450 | A02 | 12783320 | C | T | missense_variant | MODERATE | c.109C>T|p.Leu37Phe |
S175 |
| 185916 | BAA02g23450 | A02 | 12783570 | C | T | missense_variant | MODERATE | c.359C>T|p.Ser120Phe |
S286 |
| 185917 | BAA02g23450 | A02 | 12783722 | G | A | missense_variant | MODERATE | c.511G>A|p.Glu171Lys |
S247 |
| 185918 | BAA02g23460 | A02 | 12787071 | C | T | synonymous_variant | LOW | c.96C>T|p.Leu32Leu |
S71 |
| 185919 | BAA02g23460 | A02 | 12787505 | G | A | missense_variant | MODERATE | c.419G>A|p.Gly140Glu |
S223 |
| 185920 | BAA02g23450 | A02 | 12789252 | C | T | downstream_gene_variant | MODIFIER | c.*4669C>T| |
S261 |
| 185921 | BAA02g23450 | A02 | 12789350 | G | A | downstream_gene_variant | MODIFIER | c.*4767G>A| |
S148 |
| 185922 | BAA02g23450 | A02 | 12789535 | C | T | downstream_gene_variant | MODIFIER | c.*4952C>T| |
S158 |
| 185923 | BAA02g23460 | A02 | 12790384 | G | A | downstream_gene_variant | MODIFIER | c.*2267G>A| |
S275 |
| 185924 | BAA02g23460 | A02 | 12790762 | G | A | downstream_gene_variant | MODIFIER | c.*2645G>A| |
S150 |
| 185925 | BAA02g23460 | A02 | 12790948 | G | A | downstream_gene_variant | MODIFIER | c.*2831G>A| |
S202 |