Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02400 | A02 | 1067079 | C | T | synonymous_variant | LOW | c.690G>A|p.Lys230Lys |
S203 |
2 | BAA02g02400 | A02 | 1067114 | C | T | missense_variant | MODERATE | c.655G>A|p.Asp219Asn |
S306 S308 |
3 | BAA02g02400 | A02 | 1067673 | G | A | synonymous_variant | LOW | c.96C>T|p.Ile32Ile |
S291 |
4 | BAA02g02400 | A02 | 1067763 | C | T | synonymous_variant | LOW | c.6G>A|p.Glu2Glu |
S73 |
5 | BAA02g02400 | A02 | 1072473 | G | A | upstream_gene_variant | MODIFIER | c.-4705C>T| |
S238 |