Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02230 | A02 | 1001798 | C | T | synonymous_variant | LOW | c.2691G>A|p.Lys897Lys |
S135 |
2 | BAA02g02230 | A02 | 1001973 | G | A | missense_variant | MODERATE | c.2516C>T|p.Ser839Phe |
S10 |
3 | BAA02g02230 | A02 | 1003709 | C | T | missense_variant | MODERATE | c.1546G>A|p.Glu516Lys |
S241 |
4 | BAA02g02230 | A02 | 1007303 | G | A | missense_variant | MODERATE | c.227C>T|p.Thr76Ile |
S244 |
5 | BAA02g02230 | A02 | 1008091 | C | T | upstream_gene_variant | MODIFIER | c.-562G>A| |
S133 |
6 | BAA02g02230 | A02 | 1008209 | G | A | upstream_gene_variant | MODIFIER | c.-680C>T| |
S162 |
7 | BAA02g02230 | A02 | 1008590 | C | T | upstream_gene_variant | MODIFIER | c.-1061G>A| |
S183 S228 |
8 | BAA02g02230 | A02 | 1009050 | C | T | upstream_gene_variant | MODIFIER | c.-1521G>A| |
S195 |