Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20150 | A02 | 10624668 | C | T | missense_variant | MODERATE | c.4G>A|p.Gly2Arg |
S152 |
2 | BAA02g20150 | A02 | 10626050 | C | T | upstream_gene_variant | MODIFIER | c.-1379G>A| |
S112 |
3 | BAA02g20150 | A02 | 10627208 | C | T | upstream_gene_variant | MODIFIER | c.-2537G>A| |
S308 |
4 | BAA02g20150 | A02 | 10627953 | C | T | upstream_gene_variant | MODIFIER | c.-3282G>A| |
S105 S106 |
5 | BAA02g20150 | A02 | 10628400 | C | T | upstream_gene_variant | MODIFIER | c.-3729G>A| |
S135 |
6 | BAA02g20150 | A02 | 10629286 | C | T | upstream_gene_variant | MODIFIER | c.-4615G>A| |
S38 |
7 | BAA02g20150 | A02 | 10629317 | G | A | upstream_gene_variant | MODIFIER | c.-4646C>T| |
S229 |
8 | BAA02g20150 | A02 | 10629357 | G | T | upstream_gene_variant | MODIFIER | c.-4686C>A| |
S199 |
9 | BAA02g20150 | A02 | 10629499 | C | T | upstream_gene_variant | MODIFIER | c.-4828G>A| |
S75 S81 |