Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11200 | A02 | 5062181 | C | T | missense_variant | MODERATE | c.910G>A|p.Ala304Thr |
S123 |
2 | BAA02g11200 | A02 | 5062208 | C | T | missense_variant | MODERATE | c.883G>A|p.Asp295Asn |
S81 S85 |
3 | BAA02g11200 | A02 | 5063258 | G | A | missense_variant | MODERATE | c.223C>T|p.Arg75Cys |
S61 |
4 | BAA02g11200 | A02 | 5066624 | C | T | upstream_gene_variant | MODIFIER | c.-3144G>A| |
S167 |
5 | BAA02g11200 | A02 | 5066757 | C | T | upstream_gene_variant | MODIFIER | c.-3277G>A| |
S292 |
6 | BAA02g11200 | A02 | 5066901 | G | A | upstream_gene_variant | MODIFIER | c.-3421C>T| |
S50 |
7 | BAA02g11200 | A02 | 5067008 | G | A | upstream_gene_variant | MODIFIER | c.-3528C>T| |
S107 |