| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 181351 | BAA02g20850 | A02 | 11086014 | G | A | upstream_gene_variant | MODIFIER | c.-1554G>A| |
S230 |
| 181352 | BAA02g20850 | A02 | 11087971 | G | A | missense_variant | MODERATE | c.404G>A|p.Arg135Lys |
S13 S140 S168 S279 S64 |
| 181353 | BAA02g20850 | A02 | 11088148 | C | T | missense_variant | MODERATE | c.581C>T|p.Ser194Phe |
S49 |
| 181354 | BAA02g20850 | A02 | 11088244 | C | T | missense_variant | MODERATE | c.677C>T|p.Ser226Leu |
S97 |
| 181355 | BAA02g20850 | A02 | 11088404 | C | T | synonymous_variant | LOW | c.837C>T|p.Asn279Asn |
S221 |
| 181356 | BAA02g20860 | A02 | 11092761 | C | T | synonymous_variant | LOW | c.84C>T|p.Leu28Leu |
S171 |
| 181357 | BAA02g20870 | A02 | 11093146 | C | T | upstream_gene_variant | MODIFIER | c.-3457C>T| |
S284 |
| 181358 | BAA02g20870 | A02 | 11093193 | G | A | upstream_gene_variant | MODIFIER | c.-3410G>A| |
S202 |
| 181359 | BAA02g20870 | A02 | 11093546 | G | A | upstream_gene_variant | MODIFIER | c.-3057G>A| |
S278 |
| 181360 | BAA02g20870 | A02 | 11093775 | G | A | upstream_gene_variant | MODIFIER | c.-2828G>A| |
S32 |
| 181361 | BAA02g20860 | A02 | 11094288 | C | T | synonymous_variant | LOW | c.411C>T|p.Ile137Ile |
S94 |
| 181362 | BAA02g20870 | A02 | 11094662 | C | T | upstream_gene_variant | MODIFIER | c.-1941C>T| |
S18 |
| 181363 | BAA02g20870 | A02 | 11095189 | G | A | upstream_gene_variant | MODIFIER | c.-1414G>A| |
S86 |
| 181364 | BAA02g20870 | A02 | 11095587 | G | A | upstream_gene_variant | MODIFIER | c.-1016G>A| |
S282 |
| 181365 | BAA02g20870 | A02 | 11096346 | G | A | upstream_gene_variant | MODIFIER | c.-257G>A| |
S288 |
| 181366 | BAA02g20870 | A02 | 11096813 | C | T | splice_region_variant&intron_variant | LOW | c.25-7C>T| |
S255 |
| 181367 | BAA02g20870 | A02 | 11096819 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.25-1G>A| |
S4 |
| 181368 | BAA02g20870 | A02 | 11097976 | C | T | missense_variant | MODERATE | c.677C>T|p.Thr226Ile |
S208 |
| 181369 | BAA02g20870 | A02 | 11099475 | C | T | missense_variant | MODERATE | c.2176C>T|p.Leu726Phe |
S211 |
| 181370 | BAA02g20880 | A02 | 11100887 | G | A | upstream_gene_variant | MODIFIER | c.-1765G>A| |
S232 |
| 181371 | BAA02g20880 | A02 | 11101965 | C | T | upstream_gene_variant | MODIFIER | c.-687C>T| |
S234 |
| 181372 | BAA02g20880 | A02 | 11103317 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.513-1G>A| |
S57 |
| 181373 | BAA02g20880 | A02 | 11103684 | T | A | synonymous_variant | LOW | c.633T>A|p.Pro211Pro |
S152 S158 S204 S215 S267 S40 S99 |
| 181374 | BAA02g20880 | A02 | 11103701 | C | A | stop_gained | HIGH | c.650C>A|p.Ser217* |
S267 |
| 181375 | BAA02g20890 | A02 | 11104010 | G | A | upstream_gene_variant | MODIFIER | c.-2729G>A| |
S72 S78 |