Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05180 | A02 | 2277686 | C | T | missense_variant | MODERATE | c.1543G>A|p.Val515Ile |
S9 |
2 | BAA02g05180 | A02 | 2278049 | G | A | missense_variant | MODERATE | c.1247C>T|p.Thr416Ile |
S184 |
3 | BAA02g05180 | A02 | 2278257 | G | A | missense_variant | MODERATE | c.1039C>T|p.Leu347Phe |
S241 |
4 | BAA02g05180 | A02 | 2278568 | G | A | missense_variant | MODERATE | c.797C>T|p.Ala266Val |
S128 |
5 | BAA02g05180 | A02 | 2278926 | C | T | missense_variant&splice_region_variant | MODERATE | c.439G>A|p.Gly147Arg |
S13 |
6 | BAA02g05180 | A02 | 2279541 | G | A | upstream_gene_variant | MODIFIER | c.-5C>T| |
S51 |
7 | BAA02g05180 | A02 | 2280979 | G | A | upstream_gene_variant | MODIFIER | c.-1443C>T| |
S153 S257 S263 |
8 | BAA02g05180 | A02 | 2281630 | G | A | upstream_gene_variant | MODIFIER | c.-2094C>T| |
S293 |
9 | BAA02g05180 | A02 | 2281994 | G | A | upstream_gene_variant | MODIFIER | c.-2458C>T| |
S185 |