Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41400 | A05 | 39589668 | C | T | downstream_gene_variant | MODIFIER | c.*937G>A| |
S204 |
2 | BAA05g41400 | A05 | 39590638 | C | T | synonymous_variant | LOW | c.1533G>A|p.Gln511Gln |
S302 |
3 | BAA05g41400 | A05 | 39590998 | C | T | missense_variant | MODERATE | c.1255G>A|p.Glu419Lys |
S185 |
4 | BAA05g41400 | A05 | 39592331 | C | T | missense_variant | MODERATE | c.592G>A|p.Ala198Thr |
S275 |
5 | BAA05g41400 | A05 | 39593133 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.212-1G>A| |
S50 |
6 | BAA05g41400 | A05 | 39594155 | C | T | upstream_gene_variant | MODIFIER | c.-402G>A| |
S47 |
7 | BAA05g41400 | A05 | 39595487 | G | A | upstream_gene_variant | MODIFIER | c.-1734C>T| |
S12 |
8 | BAA05g41400 | A05 | 39596316 | C | T | upstream_gene_variant | MODIFIER | c.-2563G>A| |
S74 |
9 | BAA05g41400 | A05 | 39596530 | C | T | upstream_gene_variant | MODIFIER | c.-2777G>A| |
S278 |
10 | BAA05g41400 | A05 | 39597014 | C | T | upstream_gene_variant | MODIFIER | c.-3261G>A| |
S14 |