Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g26390 | A04 | 26981603 | C | T | upstream_gene_variant | MODIFIER | c.-4131C>T| |
S305 |
2 | BAA04g26390 | A04 | 26983157 | C | T | upstream_gene_variant | MODIFIER | c.-2577C>T| |
S8 |
3 | BAA04g26390 | A04 | 26983672 | G | A | upstream_gene_variant | MODIFIER | c.-2062G>A| |
S179 |
4 | BAA04g26390 | A04 | 26983783 | C | T | upstream_gene_variant | MODIFIER | c.-1951C>T| |
S9 |
5 | BAA04g26390 | A04 | 26983819 | C | T | upstream_gene_variant | MODIFIER | c.-1915C>T| |
S279 |
6 | BAA04g26390 | A04 | 26984110 | C | T | upstream_gene_variant | MODIFIER | c.-1624C>T| |
S68 |
7 | BAA04g26390 | A04 | 26986060 | C | T | synonymous_variant | LOW | c.327C>T|p.Leu109Leu |
S47 |
8 | BAA04g26390 | A04 | 26986321 | G | A | synonymous_variant | LOW | c.588G>A|p.Lys196Lys |
S13 |
9 | BAA04g26390 | A04 | 26986446 | C | T | missense_variant | MODERATE | c.713C>T|p.Pro238Leu |
S151 S263 |
10 | BAA04g26390 | A04 | 26988669 | C | T | downstream_gene_variant | MODIFIER | c.*1769C>T| |
S200 |
11 | BAA04g26390 | A04 | 26988740 | G | A | downstream_gene_variant | MODIFIER | c.*1840G>A| |
S274 |
12 | BAA04g26390 | A04 | 26990963 | G | A | downstream_gene_variant | MODIFIER | c.*4063G>A| |
S209 |
13 | BAA04g26390 | A04 | 26991324 | C | T | downstream_gene_variant | MODIFIER | c.*4424C>T| |
S247 |
14 | BAA04g26390 | A04 | 26991729 | G | A | downstream_gene_variant | MODIFIER | c.*4829G>A| |
S172 |