| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g22620 | A02 | 12250281 | G | A | upstream_gene_variant | MODIFIER | c.-4461G>A| |
S48 |
| 2 | BAA02g22620 | A02 | 12250826 | C | T | upstream_gene_variant | MODIFIER | c.-3916C>T| |
S171 |
| 3 | BAA02g22620 | A02 | 12251663 | G | A | upstream_gene_variant | MODIFIER | c.-3079G>A| |
S176 |
| 4 | BAA02g22620 | A02 | 12252412 | G | A | upstream_gene_variant | MODIFIER | c.-2330G>A| |
S230 |
| 5 | BAA02g22620 | A02 | 12253128 | G | A | upstream_gene_variant | MODIFIER | c.-1614G>A| |
S17 |
| 6 | BAA02g22620 | A02 | 12253606 | C | T | upstream_gene_variant | MODIFIER | c.-1136C>T| |
S13 S168 S239 S279 |
| 7 | BAA02g22620 | A02 | 12253740 | G | A | upstream_gene_variant | MODIFIER | c.-1002G>A| |
S47 |
| 8 | BAA02g22620 | A02 | 12254421 | G | A | upstream_gene_variant | MODIFIER | c.-321G>A| |
S172 |
| 9 | BAA02g22620 | A02 | 12254992 | C | T | intron_variant | MODIFIER | c.139+18C>T| |
S8 |
| 10 | BAA02g22620 | A02 | 12255007 | G | A | intron_variant | MODIFIER | c.139+33G>A| |
S251 |
| 11 | BAA02g22620 | A02 | 12255478 | G | A | missense_variant | MODERATE | c.491G>A|p.Gly164Glu |
S247 |
| 12 | BAA02g22620 | A02 | 12256527 | G | A | missense_variant | MODERATE | c.1192G>A|p.Glu398Lys |
S70 |
| 13 | BAA02g22620 | A02 | 12256592 | G | A | synonymous_variant | LOW | c.1257G>A|p.Glu419Glu |
S189 |
| 14 | BAA02g22620 | A02 | 12256915 | C | T | missense_variant | MODERATE | c.1421C>T|p.Ser474Phe |
S240 |
| 15 | BAA02g22620 | A02 | 12257372 | C | T | synonymous_variant | LOW | c.1683C>T|p.Val561Val |
S209 |
| 16 | BAA02g22620 | A02 | 12258338 | G | A | missense_variant | MODERATE | c.2297G>A|p.Arg766Gln |
S156 |
| 17 | BAA02g22620 | A02 | 12258718 | G | A | missense_variant&splice_region_variant | MODERATE | c.2459G>A|p.Gly820Glu |
S256 |
| 18 | BAA02g22620 | A02 | 12259800 | G | A | missense_variant | MODERATE | c.3376G>A|p.Glu1126Lys |
S17 |