| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 182751 | BAA02g21610-BAA02g21620 | A02 | 11626556 | G | A | intergenic_region | MODIFIER | n.11626556G>A| |
S4 |
| 182752 | BAA02g21620 | A02 | 11628527 | G | C | upstream_gene_variant | MODIFIER | c.-4370G>C| |
S259 |
| 182753 | BAA02g21620 | A02 | 11630448 | G | A | upstream_gene_variant | MODIFIER | c.-2449G>A| |
S230 |
| 182754 | BAA02g21620 | A02 | 11630929 | G | A | upstream_gene_variant | MODIFIER | c.-1968G>A| |
S13 |
| 182755 | BAA02g21620 | A02 | 11631422 | G | A | upstream_gene_variant | MODIFIER | c.-1475G>A| |
S136 |
| 182756 | BAA02g21620 | A02 | 11632753 | C | T | upstream_gene_variant | MODIFIER | c.-144C>T| |
S78 S83 |
| 182757 | BAA02g21620 | A02 | 11633015 | C | T | missense_variant | MODERATE | c.119C>T|p.Thr40Ile |
S289 S290 |
| 182758 | BAA02g21630 | A02 | 11633050 | C | T | downstream_gene_variant | MODIFIER | c.*1020G>A| |
S41 |
| 182759 | BAA02g21630 | A02 | 11634580 | G | A | synonymous_variant | LOW | c.1335C>T|p.Ala445Ala |
S236 |
| 182760 | BAA02g21630 | A02 | 11635305 | G | A | synonymous_variant | LOW | c.1104C>T|p.Pro368Pro |
S108 |
| 182761 | BAA02g21630 | A02 | 11635359 | C | T | synonymous_variant | LOW | c.1050G>A|p.Arg350Arg |
S249 |
| 182762 | BAA02g21630 | A02 | 11636036 | C | T | missense_variant | MODERATE | c.622G>A|p.Val208Met |
S171 |
| 182763 | BAA02g21630 | A02 | 11636744 | C | T | synonymous_variant | LOW | c.120G>A|p.Pro40Pro |
S266 |
| 182764 | BAA02g21630 | A02 | 11636771 | G | A | synonymous_variant | LOW | c.93C>T|p.Tyr31Tyr |
S134 |
| 182765 | BAA02g21630 | A02 | 11638076 | C | T | upstream_gene_variant | MODIFIER | c.-1213G>A| |
S163 |
| 182766 | BAA02g21630 | A02 | 11638705 | G | A | upstream_gene_variant | MODIFIER | c.-1842C>T| |
S45 |
| 182767 | BAA02g21630 | A02 | 11638714 | G | A | upstream_gene_variant | MODIFIER | c.-1851C>T| |
S303 |
| 182768 | BAA02g21630 | A02 | 11638729 | G | A | upstream_gene_variant | MODIFIER | c.-1866C>T| |
S69 |
| 182769 | BAA02g21630 | A02 | 11639175 | G | A | upstream_gene_variant | MODIFIER | c.-2312C>T| |
S81 S85 |
| 182770 | BAA02g21640 | A02 | 11640986 | A | T | stop_gained | HIGH | c.207T>A|p.Tyr69* |
S59 |
| 182771 | BAA02g21630 | A02 | 11641402 | C | T | upstream_gene_variant | MODIFIER | c.-4539G>A| |
S42 |
| 182772 | BAA02g21630 | A02 | 11641648 | G | A | upstream_gene_variant | MODIFIER | c.-4785C>T| |
S293 |
| 182773 | BAA02g21630 | A02 | 11641727 | A | C | upstream_gene_variant | MODIFIER | c.-4864T>G| |
S268 |
| 182774 | BAA02g21630 | A02 | 11641767 | G | A | upstream_gene_variant | MODIFIER | c.-4904C>T| |
S146 |
| 182775 | BAA02g21640 | A02 | 11641916 | C | T | upstream_gene_variant | MODIFIER | c.-724G>A| |
S123 |