| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164301 | BAA02g10850 | A02 | 4852405 | G | A | synonymous_variant | LOW | c.78G>A|p.Gln26Gln |
S132 S137 S215 S89 |
| 164302 | BAA02g10850 | A02 | 4852796 | G | A | synonymous_variant | LOW | c.402G>A|p.Lys134Lys |
S166 |
| 164303 | BAA02g10850 | A02 | 4853251 | G | A | downstream_gene_variant | MODIFIER | c.*395G>A| |
S308 |
| 164304 | BAA02g10860 | A02 | 4854550 | G | A | synonymous_variant | LOW | c.801C>T|p.Phe267Phe |
S177 |
| 164305 | BAA02g10860 | A02 | 4854577 | C | T | synonymous_variant | LOW | c.774G>A|p.Glu258Glu |
S128 |
| 164306 | BAA02g10860 | A02 | 4855288 | C | T | synonymous_variant | LOW | c.63G>A|p.Glu21Glu |
S242 |
| 164307 | BAA02g10860 | A02 | 4855898 | C | T | upstream_gene_variant | MODIFIER | c.-548G>A| |
S276 |
| 164308 | BAA02g10860 | A02 | 4856137 | C | T | upstream_gene_variant | MODIFIER | c.-787G>A| |
S40 S49 |
| 164309 | BAA02g10860 | A02 | 4857028 | G | A | upstream_gene_variant | MODIFIER | c.-1678C>T| |
S80 |
| 164310 | BAA02g10870 | A02 | 4857572 | G | A | synonymous_variant | LOW | c.1608C>T|p.Val536Val |
S235 |
| 164311 | BAA02g10870 | A02 | 4858365 | G | A | missense_variant | MODERATE | c.920C>T|p.Ser307Phe |
S86 |
| 164312 | BAA02g10860 | A02 | 4858696 | C | T | upstream_gene_variant | MODIFIER | c.-3346G>A| |
S128 |
| 164313 | BAA02g10860 | A02 | 4858727 | G | A | upstream_gene_variant | MODIFIER | c.-3377C>T| |
S61 |
| 164314 | BAA02g10860 | A02 | 4859935 | G | A | upstream_gene_variant | MODIFIER | c.-4585C>T| |
S10 |
| 164315 | BAA02g10870 | A02 | 4862012 | G | A | upstream_gene_variant | MODIFIER | c.-2333C>T| |
S156 |
| 164316 | BAA02g10870 | A02 | 4863589 | G | A | upstream_gene_variant | MODIFIER | c.-3910C>T| |
S203 |
| 164317 | BAA02g10870 | A02 | 4863660 | G | A | upstream_gene_variant | MODIFIER | c.-3981C>T| |
S286 |
| 164318 | BAA02g10880 | A02 | 4864254 | C | T | synonymous_variant | LOW | c.2076G>A|p.Lys692Lys |
S142 |
| 164319 | BAA02g10880 | A02 | 4866121 | A | G | synonymous_variant | LOW | c.774T>C|p.Asp258Asp |
S152 |
| 164320 | BAA02g10880 | A02 | 4866510 | G | A | intron_variant | MODIFIER | c.489-16C>T| |
S259 |
| 164321 | BAA02g10880 | A02 | 4866614 | C | T | missense_variant | MODERATE | c.451G>A|p.Gly151Ser |
S193 |
| 164322 | BAA02g10880 | A02 | 4867423 | C | T | missense_variant | MODERATE | c.137G>A|p.Ser46Asn |
S131 |
| 164323 | BAA02g10880 | A02 | 4867690 | G | A | upstream_gene_variant | MODIFIER | c.-131C>T| |
S104 |
| 164324 | BAA02g10880 | A02 | 4867733 | C | T | upstream_gene_variant | MODIFIER | c.-174G>A| |
S135 |
| 164325 | BAA02g10880 | A02 | 4869922 | C | T | upstream_gene_variant | MODIFIER | c.-2363G>A| |
S208 |