Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18880 | A02 | 9734237 | G | A | missense_variant | MODERATE | c.748G>A|p.Ala250Thr |
S19 |
2 | BAA02g18880 | A02 | 9734339 | G | A | missense_variant | MODERATE | c.850G>A|p.Gly284Arg |
S155 S211 |
3 | BAA02g18880 | A02 | 9734768 | A | G | downstream_gene_variant | MODIFIER | c.*412A>G| |
S74 |
4 | BAA02g18880 | A02 | 9737144 | G | A | downstream_gene_variant | MODIFIER | c.*2788G>A| |
S259 |
5 | BAA02g18880 | A02 | 9737443 | C | T | downstream_gene_variant | MODIFIER | c.*3087C>T| |
S127 |
6 | BAA02g18880 | A02 | 9737892 | C | T | downstream_gene_variant | MODIFIER | c.*3536C>T| |
S66 |
7 | BAA02g18880 | A02 | 9737945 | G | A | downstream_gene_variant | MODIFIER | c.*3589G>A| |
S95 |
8 | BAA02g18880 | A02 | 9738328 | G | A | downstream_gene_variant | MODIFIER | c.*3972G>A| |
S143 |
9 | BAA02g18880 | A02 | 9738554 | C | T | downstream_gene_variant | MODIFIER | c.*4198C>T| |
S32 |