Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45640 | A02 | 37310548 | G | A | synonymous_variant | LOW | c.2076C>T|p.Asn692Asn |
S72 |
2 | BAA02g45640 | A02 | 37311211 | G | A | missense_variant | MODERATE | c.1490C>T|p.Ser497Phe |
S89 |
3 | BAA02g45640 | A02 | 37311467 | G | A | missense_variant | MODERATE | c.1379C>T|p.Ala460Val |
S4 |
4 | BAA02g45640 | A02 | 37311642 | G | A | missense_variant | MODERATE | c.1270C>T|p.Arg424Cys |
S187 |
5 | BAA02g45640 | A02 | 37311699 | C | T | missense_variant | MODERATE | c.1213G>A|p.Glu405Lys |
S104 S52 |
6 | BAA02g45640 | A02 | 37313059 | C | T | missense_variant | MODERATE | c.463G>A|p.Asp155Asn |
S157 |
7 | BAA02g45640 | A02 | 37313160 | G | A | missense_variant | MODERATE | c.362C>T|p.Thr121Ile |
S168 |
8 | BAA02g45640 | A02 | 37313466 | C | T | missense_variant | MODERATE | c.56G>A|p.Gly19Glu |
S252 |
9 | BAA02g45640 | A02 | 37314673 | C | T | upstream_gene_variant | MODIFIER | c.-1152G>A| |
S208 S219 |
10 | BAA02g45640 | A02 | 37315738 | G | A | upstream_gene_variant | MODIFIER | c.-2217C>T| |
S10 |