Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18290 | A02 | 9256129 | C | T | missense_variant | MODERATE | c.920G>A|p.Gly307Glu |
S186 |
2 | BAA02g18290 | A02 | 9256436 | G | A | missense_variant | MODERATE | c.722C>T|p.Ala241Val |
S247 |
3 | BAA02g18290 | A02 | 9256719 | C | T | missense_variant | MODERATE | c.439G>A|p.Ala147Thr |
S18 |
4 | BAA02g18290 | A02 | 9259755 | G | A | upstream_gene_variant | MODIFIER | c.-2497C>T| |
S279 |
5 | BAA02g18290 | A02 | 9259922 | C | T | upstream_gene_variant | MODIFIER | c.-2664G>A| |
S94 |
6 | BAA02g18290 | A02 | 9260238 | G | A | upstream_gene_variant | MODIFIER | c.-2980C>T| |
S99 |
7 | BAA02g18290 | A02 | 9260647 | G | A | upstream_gene_variant | MODIFIER | c.-3389C>T| |
S294 |
8 | BAA02g18290 | A02 | 9260729 | C | T | upstream_gene_variant | MODIFIER | c.-3471G>A| |
S28 |
9 | BAA02g18290 | A02 | 9260864 | G | A | upstream_gene_variant | MODIFIER | c.-3606C>T| |
S184 |
10 | BAA02g18290 | A02 | 9260892 | T | A | upstream_gene_variant | MODIFIER | c.-3634A>T| |
S283 |
11 | BAA02g18290 | A02 | 9261024 | G | A | upstream_gene_variant | MODIFIER | c.-3766C>T| |
S157 |