Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21020 | A02 | 11232384 | G | A | missense_variant | MODERATE | c.659C>T|p.Thr220Ile |
S303 |
2 | BAA02g21020 | A02 | 11232443 | C | T | synonymous_variant | LOW | c.600G>A|p.Leu200Leu |
S155 S211 |
3 | BAA02g21020 | A02 | 11232589 | C | T | missense_variant | MODERATE | c.454G>A|p.Asp152Asn |
S234 |
4 | BAA02g21020 | A02 | 11233711 | G | A | upstream_gene_variant | MODIFIER | c.-669C>T| |
S10 |
5 | BAA02g21020 | A02 | 11234056 | C | T | upstream_gene_variant | MODIFIER | c.-1014G>A| |
S6 |
6 | BAA02g21020 | A02 | 11234682 | C | T | upstream_gene_variant | MODIFIER | c.-1640G>A| |
S299 |
7 | BAA02g21020 | A02 | 11237414 | C | T | upstream_gene_variant | MODIFIER | c.-4372G>A| |
S6 |
8 | BAA02g21020 | A02 | 11237491 | G | A | upstream_gene_variant | MODIFIER | c.-4449C>T| |
S223 |