Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11060 | A02 | 4993681 | C | T | missense_variant | MODERATE | c.170C>T|p.Pro57Leu |
S42 |
2 | BAA02g11060 | A02 | 4996898 | G | A | downstream_gene_variant | MODIFIER | c.*2399G>A| |
S165 |
3 | BAA02g11060 | A02 | 4997467 | G | A | downstream_gene_variant | MODIFIER | c.*2968G>A| |
S51 |
4 | BAA02g11060 | A02 | 4997658 | G | A | downstream_gene_variant | MODIFIER | c.*3159G>A| |
S136 |
5 | BAA02g11060 | A02 | 4997700 | C | T | downstream_gene_variant | MODIFIER | c.*3201C>T| |
S186 |
6 | BAA02g11060 | A02 | 4999011 | C | T | downstream_gene_variant | MODIFIER | c.*4512C>T| |
S6 |
7 | BAA02g11060 | A02 | 4999092 | G | A | downstream_gene_variant | MODIFIER | c.*4593G>A| |
S298 |