Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46520 | A02 | 37797842 | G | A | synonymous_variant | LOW | c.894C>T|p.Gly298Gly |
S191 |
2 | BAA02g46520 | A02 | 37797911 | C | T | synonymous_variant | LOW | c.825G>A|p.Lys275Lys |
S212 |
3 | BAA02g46520 | A02 | 37800039 | G | A | synonymous_variant | LOW | c.256C>T|p.Leu86Leu |
S207 |
4 | BAA02g46520 | A02 | 37800254 | C | T | missense_variant | MODERATE | c.41G>A|p.Arg14Lys |
S244 |
5 | BAA02g46520 | A02 | 37801884 | G | A | upstream_gene_variant | MODIFIER | c.-1590C>T| |
S55 |
6 | BAA02g46520 | A02 | 37802090 | G | A | upstream_gene_variant | MODIFIER | c.-1796C>T| |
S150 |
7 | BAA02g46520 | A02 | 37802952 | G | A | upstream_gene_variant | MODIFIER | c.-2658C>T| |
S211 S227 |
8 | BAA02g46520 | A02 | 37803289 | C | T | upstream_gene_variant | MODIFIER | c.-2995G>A| |
S123 |
9 | BAA02g46520 | A02 | 37803570 | C | T | upstream_gene_variant | MODIFIER | c.-3276G>A| |
S203 |
10 | BAA02g46520 | A02 | 37804037 | T | C | upstream_gene_variant | MODIFIER | c.-3743A>G| |
S105 S106 |
11 | BAA02g46520 | A02 | 37804274 | G | A | upstream_gene_variant | MODIFIER | c.-3980C>T| |
S44 |
12 | BAA02g46520 | A02 | 37804469 | G | A | upstream_gene_variant | MODIFIER | c.-4175C>T| |
S166 |
13 | BAA02g46520 | A02 | 37804637 | G | A | upstream_gene_variant | MODIFIER | c.-4343C>T| |
S238 |
14 | BAA02g46520 | A02 | 37804853 | C | T | upstream_gene_variant | MODIFIER | c.-4559G>A| |
S179 |
15 | BAA02g46520 | A02 | 37804862 | C | T | upstream_gene_variant | MODIFIER | c.-4568G>A| |
S206 S26 |