Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19150 | A02 | 9949336 | C | T | upstream_gene_variant | MODIFIER | c.-2856C>T| |
S186 |
2 | BAA02g19150 | A02 | 9950003 | G | A | upstream_gene_variant | MODIFIER | c.-2189G>A| |
S281 |
3 | BAA02g19150 | A02 | 9951000 | G | A | upstream_gene_variant | MODIFIER | c.-1192G>A| |
S19 |
4 | BAA02g19150 | A02 | 9951016 | G | A | upstream_gene_variant | MODIFIER | c.-1176G>A| |
S123 |
5 | BAA02g19150 | A02 | 9951057 | G | A | upstream_gene_variant | MODIFIER | c.-1135G>A| |
S256 |
6 | BAA02g19150 | A02 | 9951078 | C | T | upstream_gene_variant | MODIFIER | c.-1114C>T| |
S268 |
7 | BAA02g19150 | A02 | 9951533 | C | T | upstream_gene_variant | MODIFIER | c.-659C>T| |
S262 |
8 | BAA02g19150 | A02 | 9953538 | G | A | missense_variant | MODERATE | c.173G>A|p.Arg58Gln |
S109 |
9 | BAA02g19150 | A02 | 9953955 | C | T | synonymous_variant | LOW | c.423C>T|p.Leu141Leu |
S206 |
10 | BAA02g19150 | A02 | 9954638 | G | A | synonymous_variant | LOW | c.474G>A|p.Glu158Glu |
S19 |