Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22920 | A01 | 11650911 | C | T | missense_variant | MODERATE | c.656G>A|p.Gly219Glu |
S90 |
2 | BAA01g22920 | A01 | 11650991 | C | T | synonymous_variant | LOW | c.576G>A|p.Thr192Thr |
S168 |
3 | BAA01g22920 | A01 | 11651052 | G | A | missense_variant | MODERATE | c.515C>T|p.Thr172Met |
S155 S211 |
4 | BAA01g22920 | A01 | 11651696 | G | A | upstream_gene_variant | MODIFIER | c.-130C>T| |
S244 |
5 | BAA01g22920 | A01 | 11654434 | G | A | upstream_gene_variant | MODIFIER | c.-2868C>T| |
S199 |
6 | BAA01g22920 | A01 | 11654464 | C | A | upstream_gene_variant | MODIFIER | c.-2898G>T| |
S162 |
7 | BAA01g22920 | A01 | 11655226 | G | A | upstream_gene_variant | MODIFIER | c.-3660C>T| |
S293 |
8 | BAA01g22920 | A01 | 11655734 | G | A | upstream_gene_variant | MODIFIER | c.-4168C>T| |
S278 |
9 | BAA01g22920 | A01 | 11655807 | G | A | upstream_gene_variant | MODIFIER | c.-4241C>T| |
S262 |