| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g05340 | A07 | 4719458 | G | A | downstream_gene_variant | MODIFIER | c.*1446C>T| |
S83 S88 |
| 2 | BAA07g05340 | A07 | 4720108 | C | T | downstream_gene_variant | MODIFIER | c.*796G>A| |
S161 |
| 3 | BAA07g05340 | A07 | 4720932 | C | T | missense_variant | MODERATE | c.632G>A|p.Gly211Glu |
S274 |
| 4 | BAA07g05340 | A07 | 4721123 | C | T | synonymous_variant | LOW | c.441G>A|p.Lys147Lys |
S77 |
| 5 | BAA07g05340 | A07 | 4721154 | T | C | missense_variant | MODERATE | c.410A>G|p.His137Arg |
S27 |
| 6 | BAA07g05340 | A07 | 4721470 | C | T | missense_variant | MODERATE | c.256G>A|p.Val86Ile |
S150 |
| 7 | BAA07g05340 | A07 | 4721601 | G | A | missense_variant | MODERATE | c.125C>T|p.Thr42Ile |
S25 |
| 8 | BAA07g05340 | A07 | 4721675 | G | A | synonymous_variant | LOW | c.51C>T|p.Arg17Arg |
S83 S88 |
| 9 | BAA07g05340 | A07 | 4721747 | G | A | upstream_gene_variant | MODIFIER | c.-22C>T| |
S151 |
| 10 | BAA07g05340 | A07 | 4721802 | C | T | upstream_gene_variant | MODIFIER | c.-77G>A| |
S150 |
| 11 | BAA07g05340 | A07 | 4722145 | G | A | upstream_gene_variant | MODIFIER | c.-420C>T| |
S200 |
| 12 | BAA07g05340 | A07 | 4722229 | C | T | upstream_gene_variant | MODIFIER | c.-504G>A| |
S294 |
| 13 | BAA07g05340 | A07 | 4723793 | G | A | upstream_gene_variant | MODIFIER | c.-2068C>T| |
S2 |
| 14 | BAA07g05340 | A07 | 4725341 | C | T | upstream_gene_variant | MODIFIER | c.-3616G>A| |
S156 |
| 15 | BAA07g05340 | A07 | 4725387 | C | T | upstream_gene_variant | MODIFIER | c.-3662G>A| |
S37 |
| 16 | BAA07g05340 | A07 | 4725525 | C | T | upstream_gene_variant | MODIFIER | c.-3800G>A| |
S256 |
| 17 | BAA07g05340 | A07 | 4725688 | G | A | upstream_gene_variant | MODIFIER | c.-3963C>T| |
S159 S243 S299 |
| 18 | BAA07g05340 | A07 | 4726196 | G | A | upstream_gene_variant | MODIFIER | c.-4471C>T| |
S54 |
| 19 | BAA07g05340 | A07 | 4726308 | C | T | upstream_gene_variant | MODIFIER | c.-4583G>A| |
S23 |