| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g00490 | A05 | 257265 | C | T | missense_variant | MODERATE | c.514G>A|p.Gly172Ser |
S202 |
| 2 | BAA05g00490 | A05 | 257933 | C | T | synonymous_variant | LOW | c.273G>A|p.Lys91Lys |
S112 |
| 3 | BAA05g00490 | A05 | 258308 | C | T | synonymous_variant | LOW | c.108G>A|p.Glu36Glu |
S124 |
| 4 | BAA05g00490 | A05 | 258310 | C | T | missense_variant | MODERATE | c.106G>A|p.Glu36Lys |
S197 |
| 5 | BAA05g00490 | A05 | 258431 | G | A | upstream_gene_variant | MODIFIER | c.-16C>T| |
S282 |
| 6 | BAA05g00490 | A05 | 258739 | C | T | upstream_gene_variant | MODIFIER | c.-324G>A| |
S281 |
| 7 | BAA05g00490 | A05 | 259079 | G | A | upstream_gene_variant | MODIFIER | c.-664C>T| |
S282 |
| 8 | BAA05g00490 | A05 | 259083 | C | T | upstream_gene_variant | MODIFIER | c.-668G>A| |
S259 |
| 9 | BAA05g00490 | A05 | 259267 | C | T | upstream_gene_variant | MODIFIER | c.-852G>A| |
S4 |
| 10 | BAA05g00490 | A05 | 261196 | C | T | upstream_gene_variant | MODIFIER | c.-2781G>A| |
S25 |
| 11 | BAA05g00490 | A05 | 261422 | C | T | upstream_gene_variant | MODIFIER | c.-3007G>A| |
S308 |
| 12 | BAA05g00490 | A05 | 261897 | G | A | upstream_gene_variant | MODIFIER | c.-3482C>T| |
S306 S308 |
| 13 | BAA05g00490 | A05 | 262140 | G | A | upstream_gene_variant | MODIFIER | c.-3725C>T| |
S179 |
| 14 | BAA05g00490 | A05 | 262878 | C | T | upstream_gene_variant | MODIFIER | c.-4463G>A| |
S195 |
| 15 | BAA05g00490 | A05 | 263214 | C | T | upstream_gene_variant | MODIFIER | c.-4799G>A| |
S204 |