Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20850 | A02 | 11082733 | C | T | upstream_gene_variant | MODIFIER | c.-4835C>T| |
S66 |
2 | BAA02g20850 | A02 | 11084077 | C | T | upstream_gene_variant | MODIFIER | c.-3491C>T| |
S221 |
3 | BAA02g20850 | A02 | 11084424 | C | T | upstream_gene_variant | MODIFIER | c.-3144C>T| |
S179 |
4 | BAA02g20850 | A02 | 11084907 | C | T | upstream_gene_variant | MODIFIER | c.-2661C>T| |
S299 |
5 | BAA02g20850 | A02 | 11085705 | C | T | upstream_gene_variant | MODIFIER | c.-1863C>T| |
S266 |
6 | BAA02g20850 | A02 | 11085880 | C | T | upstream_gene_variant | MODIFIER | c.-1688C>T| |
S138 |
7 | BAA02g20850 | A02 | 11086014 | G | A | upstream_gene_variant | MODIFIER | c.-1554G>A| |
S230 |
8 | BAA02g20850 | A02 | 11087971 | G | A | missense_variant | MODERATE | c.404G>A|p.Arg135Lys |
S13 S140 S168 S279 S64 |
9 | BAA02g20850 | A02 | 11088148 | C | T | missense_variant | MODERATE | c.581C>T|p.Ser194Phe |
S49 |
10 | BAA02g20850 | A02 | 11088244 | C | T | missense_variant | MODERATE | c.677C>T|p.Ser226Leu |
S97 |
11 | BAA02g20850 | A02 | 11088404 | C | T | synonymous_variant | LOW | c.837C>T|p.Asn279Asn |
S221 |