Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11280 | A02 | 5092266 | G | A | upstream_gene_variant | MODIFIER | c.-4932G>A| |
S187 |
2 | BAA02g11280 | A02 | 5092941 | C | T | upstream_gene_variant | MODIFIER | c.-4257C>T| |
S182 |
3 | BAA02g11280 | A02 | 5093571 | G | A | upstream_gene_variant | MODIFIER | c.-3627G>A| |
S229 |
4 | BAA02g11280 | A02 | 5094604 | C | T | upstream_gene_variant | MODIFIER | c.-2594C>T| |
S249 |
5 | BAA02g11280 | A02 | 5094738 | T | G | upstream_gene_variant | MODIFIER | c.-2460T>G| |
S17 |
6 | BAA02g11280 | A02 | 5094848 | G | A | upstream_gene_variant | MODIFIER | c.-2350G>A| |
S205 |
7 | BAA02g11280 | A02 | 5095133 | C | T | upstream_gene_variant | MODIFIER | c.-2065C>T| |
S186 |
8 | BAA02g11280 | A02 | 5095435 | C | T | upstream_gene_variant | MODIFIER | c.-1763C>T| |
S123 S99 |
9 | BAA02g11280 | A02 | 5095574 | G | A | upstream_gene_variant | MODIFIER | c.-1624G>A| |
S282 |
10 | BAA02g11280 | A02 | 5095920 | G | A | upstream_gene_variant | MODIFIER | c.-1278G>A| |
S229 |
11 | BAA02g11280 | A02 | 5097870 | G | A | missense_variant | MODERATE | c.445G>A|p.Asp149Asn |
S204 |
12 | BAA02g11280 | A02 | 5098673 | G | A | downstream_gene_variant | MODIFIER | c.*257G>A| |
S206 S26 |
13 | BAA02g11280 | A02 | 5099390 | G | A | downstream_gene_variant | MODIFIER | c.*974G>A| |
S92 |