Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g36190 | A09 | 44500748 | C | T | intron_variant | MODIFIER | c.1045+117G>A| |
S186 S301 |
2 | BAA09g36190 | A09 | 44500758 | A | G | intron_variant | MODIFIER | c.1045+107T>C| |
S109 |
3 | BAA09g36190 | A09 | 44501666 | G | A | missense_variant | MODERATE | c.409C>T|p.Leu137Phe |
S260 |
4 | BAA09g36190 | A09 | 44503806 | G | A | upstream_gene_variant | MODIFIER | c.-1732C>T| |
S88 |
5 | BAA09g36190 | A09 | 44503884 | C | T | upstream_gene_variant | MODIFIER | c.-1810G>A| |
S174 S27 |
6 | BAA09g36190 | A09 | 44503990 | G | A | upstream_gene_variant | MODIFIER | c.-1916C>T| |
S221 |
7 | BAA09g36190 | A09 | 44504841 | C | T | upstream_gene_variant | MODIFIER | c.-2767G>A| |
S68 |
8 | BAA09g36190 | A09 | 44506158 | C | T | upstream_gene_variant | MODIFIER | c.-4084G>A| |
S122 |
9 | BAA09g36190 | A09 | 44506792 | G | A | upstream_gene_variant | MODIFIER | c.-4718C>T| |
S45 |