| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156201 | BAA02g04260 | A02 | 1860165 | G | A | downstream_gene_variant | MODIFIER | c.*4463G>A| |
S166 |
| 156202 | BAA02g04260-BAA02g04270 | A02 | 1860982 | C | T | intergenic_region | MODIFIER | n.1860982C>T| |
S255 |
| 156203 | BAA02g04270 | A02 | 1864866 | G | A | upstream_gene_variant | MODIFIER | c.-2707G>A| |
S210 |
| 156204 | BAA02g04270 | A02 | 1865461 | C | T | upstream_gene_variant | MODIFIER | c.-2112C>T| |
S66 |
| 156205 | BAA02g04270 | A02 | 1865766 | C | T | upstream_gene_variant | MODIFIER | c.-1807C>T| |
S55 |
| 156206 | BAA02g04270 | A02 | 1867132 | G | A | upstream_gene_variant | MODIFIER | c.-441G>A| |
S223 |
| 156207 | BAA02g04270 | A02 | 1868873 | C | T | missense_variant | MODERATE | c.872C>T|p.Ser291Phe |
S167 |
| 156208 | BAA02g04270 | A02 | 1869770 | G | A | missense_variant | MODERATE | c.1769G>A|p.Arg590Lys |
S239 |
| 156209 | BAA02g04270 | A02 | 1869801 | G | A | synonymous_variant | LOW | c.1800G>A|p.Arg600Arg |
S52 |
| 156210 | BAA02g04270 | A02 | 1870602 | G | A | synonymous_variant | LOW | c.2601G>A|p.Gly867Gly |
S188 |
| 156211 | BAA02g04280 | A02 | 1872011 | G | A | synonymous_variant | LOW | c.1206C>T|p.Asp402Asp |
S45 |
| 156212 | BAA02g04270 | A02 | 1872315 | C | T | downstream_gene_variant | MODIFIER | c.*1404C>T| |
S18 |
| 156213 | BAA02g04270 | A02 | 1872775 | C | T | downstream_gene_variant | MODIFIER | c.*1864C>T| |
S54 |
| 156214 | BAA02g04280 | A02 | 1873884 | G | A | upstream_gene_variant | MODIFIER | c.-74C>T| |
S68 |
| 156215 | BAA02g04280 | A02 | 1874100 | C | T | upstream_gene_variant | MODIFIER | c.-290G>A| |
S240 |
| 156216 | BAA02g04280 | A02 | 1874475 | C | T | upstream_gene_variant | MODIFIER | c.-665G>A| |
S15 S3 |
| 156217 | BAA02g04280 | A02 | 1876333 | C | T | upstream_gene_variant | MODIFIER | c.-2523G>A| |
S94 |
| 156218 | BAA02g04280 | A02 | 1876904 | G | A | upstream_gene_variant | MODIFIER | c.-3094C>T| |
S241 |
| 156219 | BAA02g04290 | A02 | 1877025 | C | T | synonymous_variant | LOW | c.852G>A|p.Gly284Gly |
S131 |
| 156220 | BAA02g04290 | A02 | 1877088 | C | T | synonymous_variant | LOW | c.789G>A|p.Ala263Ala |
S42 |
| 156221 | BAA02g04290 | A02 | 1877293 | G | A | missense_variant | MODERATE | c.584C>T|p.Ala195Val |
S63 |
| 156222 | BAA02g04290 | A02 | 1877485 | G | A | missense_variant | MODERATE | c.392C>T|p.Ser131Phe |
S64 |
| 156223 | BAA02g04290 | A02 | 1877514 | G | A | synonymous_variant | LOW | c.363C>T|p.Leu121Leu |
S279 |
| 156224 | BAA02g04290 | A02 | 1877562 | G | A | synonymous_variant | LOW | c.315C>T|p.His105His |
S239 |
| 156225 | BAA02g04290 | A02 | 1877592 | G | A | synonymous_variant | LOW | c.285C>T|p.Leu95Leu |
S239 |