Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20490 | A02 | 10871101 | C | T | upstream_gene_variant | MODIFIER | c.-3859C>T| |
S53 |
2 | BAA02g20490 | A02 | 10873438 | G | A | upstream_gene_variant | MODIFIER | c.-1522G>A| |
S149 |
3 | BAA02g20490 | A02 | 10874803 | C | T | upstream_gene_variant | MODIFIER | c.-157C>T| |
S8 |
4 | BAA02g20490 | A02 | 10874975 | G | A | missense_variant | MODERATE | c.16G>A|p.Val6Ile |
S136 |
5 | BAA02g20490 | A02 | 10875005 | G | A | missense_variant | MODERATE | c.46G>A|p.Gly16Arg |
S284 S295 |
6 | BAA02g20490 | A02 | 10875969 | G | A | synonymous_variant | LOW | c.501G>A|p.Lys167Lys |
S79 S91 |
7 | BAA02g20490 | A02 | 10876652 | G | A | synonymous_variant | LOW | c.663G>A|p.Pro221Pro |
S150 |
8 | BAA02g20490 | A02 | 10877787 | G | A | missense_variant | MODERATE | c.1081G>A|p.Ala361Thr |
S72 |
9 | BAA02g20490 | A02 | 10878120 | G | A | synonymous_variant | LOW | c.1341G>A|p.Arg447Arg |
S136 |
10 | BAA02g20490 | A02 | 10879372 | C | T | downstream_gene_variant | MODIFIER | c.*169C>T| |
S118 |