Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44960 | A02 | 36923299 | G | A | synonymous_variant | LOW | c.412C>T|p.Leu138Leu |
S229 |
2 | BAA02g44960 | A02 | 36924362 | G | A | intron_variant | MODIFIER | c.91+37C>T| |
S44 |
3 | BAA02g44960 | A02 | 36924364 | G | A | intron_variant | MODIFIER | c.91+35C>T| |
S174 S27 |
4 | BAA02g44960 | A02 | 36924413 | G | A | missense_variant | MODERATE | c.77C>T|p.Ser26Phe |
S239 |
5 | BAA02g44960 | A02 | 36924418 | C | T | synonymous_variant | LOW | c.72G>A|p.Leu24Leu |
S171 |
6 | BAA02g44960 | A02 | 36925250 | G | A | upstream_gene_variant | MODIFIER | c.-761C>T| |
S28 |
7 | BAA02g44960 | A02 | 36925572 | C | T | upstream_gene_variant | MODIFIER | c.-1083G>A| |
S303 |
8 | BAA02g44960 | A02 | 36927062 | G | A | upstream_gene_variant | MODIFIER | c.-2573C>T| |
S4 |
9 | BAA02g44960 | A02 | 36927470 | C | T | upstream_gene_variant | MODIFIER | c.-2981G>A| |
S144 |
10 | BAA02g44960 | A02 | 36928089 | C | T | upstream_gene_variant | MODIFIER | c.-3600G>A| |
S263 |
11 | BAA02g44960 | A02 | 36928191 | G | A | upstream_gene_variant | MODIFIER | c.-3702C>T| |
S72 |