Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46880 | A02 | 37971944 | G | A | synonymous_variant | LOW | c.1947C>T|p.Ile649Ile |
S80 |
2 | BAA02g46880 | A02 | 37972042 | G | A | missense_variant | MODERATE | c.1849C>T|p.Pro617Ser |
S30 |
3 | BAA02g46880 | A02 | 37972272 | G | A | missense_variant | MODERATE | c.1619C>T|p.Ala540Val |
S207 |
4 | BAA02g46880 | A02 | 37976472 | G | A | missense_variant&splice_region_variant | MODERATE | c.574C>T|p.Arg192Trp |
S68 |
5 | BAA02g46880 | A02 | 37978039 | C | T | upstream_gene_variant | MODIFIER | c.-830G>A| |
S17 |
6 | BAA02g46880 | A02 | 37978164 | C | T | upstream_gene_variant | MODIFIER | c.-955G>A| |
S205 |
7 | BAA02g46880 | A02 | 37978299 | C | T | upstream_gene_variant | MODIFIER | c.-1090G>A| |
S244 |
8 | BAA02g46880 | A02 | 37978411 | G | A | upstream_gene_variant | MODIFIER | c.-1202C>T| |
S66 |
9 | BAA02g46880 | A02 | 37979411 | G | A | upstream_gene_variant | MODIFIER | c.-2202C>T| |
S132 S137 S215 S89 |
10 | BAA02g46880 | A02 | 37980142 | C | T | upstream_gene_variant | MODIFIER | c.-2933G>A| |
S189 |
11 | BAA02g46880 | A02 | 37980447 | G | A | upstream_gene_variant | MODIFIER | c.-3238C>T| |
S251 |