Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11870 | A02 | 5355238 | C | T | missense_variant | MODERATE | c.493G>A|p.Val165Ile |
S289 S290 |
2 | BAA02g11870 | A02 | 5358815 | C | T | upstream_gene_variant | MODIFIER | c.-2630G>A| |
S257 |
3 | BAA02g11870 | A02 | 5359471 | G | A | upstream_gene_variant | MODIFIER | c.-3286C>T| |
S51 |
4 | BAA02g11870 | A02 | 5360192 | C | T | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S183 S198 |
5 | BAA02g11870 | A02 | 5360206 | C | T | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S120 |
6 | BAA02g11870 | A02 | 5360426 | G | A | upstream_gene_variant | MODIFIER | c.-4241C>T| |
S295 |
7 | BAA02g11870 | A02 | 5360563 | C | T | upstream_gene_variant | MODIFIER | c.-4378G>A| |
S299 |
8 | BAA02g11870 | A02 | 5360768 | G | A | upstream_gene_variant | MODIFIER | c.-4583C>T| |
S207 |
9 | BAA02g11870 | A02 | 5360999 | C | T | upstream_gene_variant | MODIFIER | c.-4814G>A| |
S128 |