Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22220 | A02 | 11962046 | C | T | synonymous_variant | LOW | c.774G>A|p.Leu258Leu |
S6 |
2 | BAA02g22220 | A02 | 11962210 | G | A | missense_variant | MODERATE | c.610C>T|p.Pro204Ser |
S47 |
3 | BAA02g22220 | A02 | 11964197 | C | T | upstream_gene_variant | MODIFIER | c.-1378G>A| |
S273 |
4 | BAA02g22220 | A02 | 11964470 | C | T | upstream_gene_variant | MODIFIER | c.-1651G>A| |
S121 |
5 | BAA02g22220 | A02 | 11965100 | C | T | upstream_gene_variant | MODIFIER | c.-2281G>A| |
S80 |
6 | BAA02g22220 | A02 | 11965194 | G | A | upstream_gene_variant | MODIFIER | c.-2375C>T| |
S188 |
7 | BAA02g22220 | A02 | 11965501 | C | T | upstream_gene_variant | MODIFIER | c.-2682G>A| |
S140 |
8 | BAA02g22220 | A02 | 11965864 | G | A | upstream_gene_variant | MODIFIER | c.-3045C>T| |
S205 |
9 | BAA02g22220 | A02 | 11966729 | G | A | upstream_gene_variant | MODIFIER | c.-3910C>T| |
S132 S137 S215 S263 |
10 | BAA02g22220 | A02 | 11966749 | C | T | upstream_gene_variant | MODIFIER | c.-3930G>A| |
S193 |
11 | BAA02g22220 | A02 | 11966960 | G | A | upstream_gene_variant | MODIFIER | c.-4141C>T| |
S229 |