Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g44630 | A03 | 21239448 | G | A | upstream_gene_variant | MODIFIER | c.-4893G>A| |
S260 |
2 | BAA03g44630 | A03 | 21239931 | C | T | upstream_gene_variant | MODIFIER | c.-4410C>T| |
S2 |
3 | BAA03g44630 | A03 | 21241457 | G | A | upstream_gene_variant | MODIFIER | c.-2884G>A| |
S130 |
4 | BAA03g44630 | A03 | 21241857 | G | A | upstream_gene_variant | MODIFIER | c.-2484G>A| |
S271 |
5 | BAA03g44630 | A03 | 21242039 | G | A | upstream_gene_variant | MODIFIER | c.-2302G>A| |
S70 |
6 | BAA03g44630 | A03 | 21242117 | G | A | upstream_gene_variant | MODIFIER | c.-2224G>A| |
S260 |
7 | BAA03g44630 | A03 | 21243754 | C | T | upstream_gene_variant | MODIFIER | c.-587C>T| |
S224 |
8 | BAA03g44630 | A03 | 21244028 | G | A | upstream_gene_variant | MODIFIER | c.-313G>A| |
S85 |
9 | BAA03g44630 | A03 | 21244452 | C | T | missense_variant | MODERATE | c.112C>T|p.Pro38Ser |
S241 |
10 | BAA03g44630 | A03 | 21244868 | G | A | downstream_gene_variant | MODIFIER | c.*330G>A| |
S160 |
11 | BAA03g44630 | A03 | 21245549 | G | A | downstream_gene_variant | MODIFIER | c.*1011G>A| |
S5 |
12 | BAA03g44630 | A03 | 21248075 | G | A | downstream_gene_variant | MODIFIER | c.*3537G>A| |
S168 |
13 | BAA03g44630 | A03 | 21249465 | G | A | downstream_gene_variant | MODIFIER | c.*4927G>A| |
S261 |