| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 179301 | BAA02g19780 | A02 | 10340108 | G | A | missense_variant | MODERATE | c.71C>T|p.Pro24Leu |
S19 |
| 179302 | BAA02g19780 | A02 | 10340237 | C | T | upstream_gene_variant | MODIFIER | c.-59G>A| |
S100 |
| 179303 | BAA02g19780 | A02 | 10341699 | G | A | upstream_gene_variant | MODIFIER | c.-1521C>T| |
S287 |
| 179304 | BAA02g19780 | A02 | 10342245 | G | A | upstream_gene_variant | MODIFIER | c.-2067C>T| |
S193 |
| 179305 | BAA02g19780 | A02 | 10343866 | G | A | upstream_gene_variant | MODIFIER | c.-3688C>T| |
S92 |
| 179306 | BAA02g19790 | A02 | 10344073 | C | T | synonymous_variant | LOW | c.777G>A|p.Leu259Leu |
S283 |
| 179307 | BAA02g19790 | A02 | 10344214 | C | T | synonymous_variant | LOW | c.636G>A|p.Glu212Glu |
S164 |
| 179308 | BAA02g19790 | A02 | 10344527 | G | A | missense_variant | MODERATE | c.323C>T|p.Ser108Leu |
S41 |
| 179309 | BAA02g19790 | A02 | 10344594 | G | A | missense_variant | MODERATE | c.256C>T|p.Arg86Trp |
S35 |
| 179310 | BAA02g19790 | A02 | 10345290 | C | T | upstream_gene_variant | MODIFIER | c.-441G>A| |
|
| 179311 | BAA02g19790 | A02 | 10346831 | G | A | upstream_gene_variant | MODIFIER | c.-1982C>T| |
S169 |
| 179312 | BAA02g19790 | A02 | 10347420 | C | T | upstream_gene_variant | MODIFIER | c.-2571G>A| |
S301 S304 |
| 179313 | BAA02g19790 | A02 | 10349343 | C | T | upstream_gene_variant | MODIFIER | c.-4494G>A| |
S202 |
| 179314 | BAA02g19790 | A02 | 10349630 | G | A | upstream_gene_variant | MODIFIER | c.-4781C>T| |
S247 |
| 179315 | BAA02g19800 | A02 | 10351623 | G | A | upstream_gene_variant | MODIFIER | c.-558C>T| |
S125 |
| 179316 | BAA02g19800 | A02 | 10351736 | C | T | upstream_gene_variant | MODIFIER | c.-671G>A| |
S218 |
| 179317 | BAA02g19800 | A02 | 10353038 | C | T | upstream_gene_variant | MODIFIER | c.-1973G>A| |
S266 |
| 179318 | BAA02g19800 | A02 | 10354578 | G | A | upstream_gene_variant | MODIFIER | c.-3513C>T| |
S107 |
| 179319 | BAA02g19800 | A02 | 10354621 | C | T | upstream_gene_variant | MODIFIER | c.-3556G>A| |
S230 |
| 179320 | BAA02g19800 | A02 | 10355940 | G | A | upstream_gene_variant | MODIFIER | c.-4875C>T| |
S129 |
| 179321 | BAA02g19800-BAA02g19810 | A02 | 10356382 | G | A | intergenic_region | MODIFIER | n.10356382G>A| |
S298 |
| 179322 | BAA02g19810 | A02 | 10356776 | G | A | downstream_gene_variant | MODIFIER | c.*4614C>T| |
S122 |
| 179323 | BAA02g19810 | A02 | 10357190 | C | T | downstream_gene_variant | MODIFIER | c.*4200G>A| |
S54 |
| 179324 | BAA02g19810 | A02 | 10357760 | G | A | downstream_gene_variant | MODIFIER | c.*3630C>T| |
S92 |
| 179325 | BAA02g19810 | A02 | 10357875 | C | T | downstream_gene_variant | MODIFIER | c.*3515G>A| |
S226 |