Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17890 | A02 | 8955252 | C | T | upstream_gene_variant | MODIFIER | c.-3996C>T| |
S171 |
2 | BAA02g17890 | A02 | 8956103 | G | A | upstream_gene_variant | MODIFIER | c.-3145G>A| |
S157 |
3 | BAA02g17890 | A02 | 8956953 | G | A | upstream_gene_variant | MODIFIER | c.-2295G>A| |
S289 S290 |
4 | BAA02g17890 | A02 | 8957513 | C | T | upstream_gene_variant | MODIFIER | c.-1735C>T| |
S105 S106 |
5 | BAA02g17890 | A02 | 8957734 | G | A | upstream_gene_variant | MODIFIER | c.-1514G>A| |
S294 |
6 | BAA02g17890 | A02 | 8958009 | C | T | upstream_gene_variant | MODIFIER | c.-1239C>T| |
S158 |
7 | BAA02g17890 | A02 | 8958090 | C | T | upstream_gene_variant | MODIFIER | c.-1158C>T| |
S60 |
8 | BAA02g17890 | A02 | 8959490 | C | T | synonymous_variant | LOW | c.243C>T|p.Val81Val |
S183 |
9 | BAA02g17890 | A02 | 8959605 | G | A | missense_variant | MODERATE | c.358G>A|p.Ala120Thr |
S162 |
10 | BAA02g17890 | A02 | 8959616 | G | A | synonymous_variant | LOW | c.369G>A|p.Gln123Gln |
S217 S248 |
11 | BAA02g17890 | A02 | 8960833 | C | T | downstream_gene_variant | MODIFIER | c.*977C>T| |
S201 |
12 | BAA02g17890 | A02 | 8960872 | G | A | downstream_gene_variant | MODIFIER | c.*1016G>A| |
S279 |
13 | BAA02g17890 | A02 | 8961395 | G | A | downstream_gene_variant | MODIFIER | c.*1539G>A| |
S202 |
14 | BAA02g17890 | A02 | 8961417 | C | T | downstream_gene_variant | MODIFIER | c.*1561C>T| |
S15 S3 |
15 | BAA02g17890 | A02 | 8963722 | G | A | downstream_gene_variant | MODIFIER | c.*3866G>A| |
S149 |
16 | BAA02g17890 | A02 | 8964260 | C | T | downstream_gene_variant | MODIFIER | c.*4404C>T| |
S42 |
17 | BAA02g17890 | A02 | 8964539 | G | A | downstream_gene_variant | MODIFIER | c.*4683G>A| |
S130 |