Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18890 | A02 | 9762224 | C | T | upstream_gene_variant | MODIFIER | c.-4120C>T| |
S255 |
2 | BAA02g18890 | A02 | 9762675 | G | A | upstream_gene_variant | MODIFIER | c.-3669G>A| |
S62 |
3 | BAA02g18890 | A02 | 9765061 | G | A | upstream_gene_variant | MODIFIER | c.-1283G>A| |
S122 S221 |
4 | BAA02g18890 | A02 | 9765783 | C | T | upstream_gene_variant | MODIFIER | c.-561C>T| |
S105 S106 |
5 | BAA02g18890 | A02 | 9766214 | G | A | upstream_gene_variant | MODIFIER | c.-130G>A| |
S296 |
6 | BAA02g18890 | A02 | 9767055 | C | T | intron_variant | MODIFIER | c.403-109C>T| |
S241 |
7 | BAA02g18890 | A02 | 9768681 | G | A | downstream_gene_variant | MODIFIER | c.*786G>A| |
S95 |
8 | BAA02g18890 | A02 | 9768887 | C | T | downstream_gene_variant | MODIFIER | c.*992C>T| |
S140 |
9 | BAA02g18890 | A02 | 9768943 | C | T | downstream_gene_variant | MODIFIER | c.*1048C>T| |
S181 S217 S248 S56 |
10 | BAA02g18890 | A02 | 9769040 | G | A | downstream_gene_variant | MODIFIER | c.*1145G>A| |
S17 |
11 | BAA02g18890 | A02 | 9769455 | G | A | downstream_gene_variant | MODIFIER | c.*1560G>A| |
S45 |
12 | BAA02g18890 | A02 | 9769614 | G | A | downstream_gene_variant | MODIFIER | c.*1719G>A| |
S45 |
13 | BAA02g18890 | A02 | 9769790 | G | A | downstream_gene_variant | MODIFIER | c.*1895G>A| |
S110 |
14 | BAA02g18890 | A02 | 9769897 | C | T | downstream_gene_variant | MODIFIER | c.*2002C>T| |
S234 |
15 | BAA02g18890 | A02 | 9770294 | G | A | downstream_gene_variant | MODIFIER | c.*2399G>A| |
S259 |