Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17830 | A02 | 8901729 | G | A | upstream_gene_variant | MODIFIER | c.-1551G>A| |
S48 |
2 | BAA02g17830 | A02 | 8903481 | G | A | splice_donor_variant&intron_variant | HIGH | c.201+1G>A| |
S19 |
3 | BAA02g17830 | A02 | 8904443 | C | T | intron_variant | MODIFIER | c.263+99C>T| |
S272 |
4 | BAA02g17830 | A02 | 8904833 | C | T | intron_variant | MODIFIER | c.263+489C>T| |
S268 |
5 | BAA02g17830 | A02 | 8905755 | G | A | missense_variant | MODERATE | c.512G>A|p.Gly171Glu |
S132 S137 S138 S215 S237 S288 S89 |
6 | BAA02g17830 | A02 | 8907749 | G | A | downstream_gene_variant | MODIFIER | c.*1978G>A| |
S217 S248 |
7 | BAA02g17830 | A02 | 8908420 | C | T | downstream_gene_variant | MODIFIER | c.*2649C>T| |
S182 |
8 | BAA02g17830 | A02 | 8908655 | G | A | downstream_gene_variant | MODIFIER | c.*2884G>A| |
S289 S290 |
9 | BAA02g17830 | A02 | 8909782 | C | T | downstream_gene_variant | MODIFIER | c.*4011C>T| |
S208 |
10 | BAA02g17830 | A02 | 8909870 | G | A | downstream_gene_variant | MODIFIER | c.*4099G>A| |
S161 |