Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18920 | A02 | 9779888 | C | T | missense_variant | MODERATE | c.520G>A|p.Ala174Thr |
S165 |
2 | BAA02g18920 | A02 | 9780014 | G | A | missense_variant&splice_region_variant | MODERATE | c.476C>T|p.Pro159Leu |
S236 |
3 | BAA02g18920 | A02 | 9784042 | C | T | upstream_gene_variant | MODIFIER | c.-1018G>A| |
S219 |
4 | BAA02g18920 | A02 | 9785408 | G | A | upstream_gene_variant | MODIFIER | c.-2384C>T| |
S173 |
5 | BAA02g18920 | A02 | 9785796 | C | T | upstream_gene_variant | MODIFIER | c.-2772G>A| |
S270 |
6 | BAA02g18920 | A02 | 9786617 | G | A | upstream_gene_variant | MODIFIER | c.-3593C>T| |
S116 |
7 | BAA02g18920 | A02 | 9786843 | G | A | upstream_gene_variant | MODIFIER | c.-3819C>T| |
S155 |
8 | BAA02g18920 | A02 | 9787016 | C | T | upstream_gene_variant | MODIFIER | c.-3992G>A| |
S138 |
9 | BAA02g18920 | A02 | 9787276 | C | T | upstream_gene_variant | MODIFIER | c.-4252G>A| |
S47 |
10 | BAA02g18920 | A02 | 9787607 | G | A | upstream_gene_variant | MODIFIER | c.-4583C>T| |
S37 |