Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19490 | A02 | 10112484 | C | T | upstream_gene_variant | MODIFIER | c.-4082C>T| |
S44 |
2 | BAA02g19490 | A02 | 10112764 | C | T | upstream_gene_variant | MODIFIER | c.-3802C>T| |
S183 S198 |
3 | BAA02g19490 | A02 | 10112841 | C | T | upstream_gene_variant | MODIFIER | c.-3725C>T| |
S179 |
4 | BAA02g19490 | A02 | 10113254 | G | A | upstream_gene_variant | MODIFIER | c.-3312G>A| |
S303 |
5 | BAA02g19490 | A02 | 10113894 | C | T | upstream_gene_variant | MODIFIER | c.-2672C>T| |
S211 S227 |
6 | BAA02g19490 | A02 | 10114005 | C | T | upstream_gene_variant | MODIFIER | c.-2561C>T| |
S142 |
7 | BAA02g19490 | A02 | 10114310 | C | T | upstream_gene_variant | MODIFIER | c.-2256C>T| |
S100 |
8 | BAA02g19490 | A02 | 10114389 | C | T | upstream_gene_variant | MODIFIER | c.-2177C>T| |
S209 |
9 | BAA02g19490 | A02 | 10115002 | G | A | upstream_gene_variant | MODIFIER | c.-1564G>A| |
S41 |
10 | BAA02g19490 | A02 | 10115830 | G | A | upstream_gene_variant | MODIFIER | c.-736G>A| |
S161 |
11 | BAA02g19490 | A02 | 10116197 | C | T | upstream_gene_variant | MODIFIER | c.-369C>T| |
S275 |
12 | BAA02g19490 | A02 | 10116748 | G | A | synonymous_variant | LOW | c.93G>A|p.Lys31Lys |
S129 |
13 | BAA02g19490 | A02 | 10117512 | G | A | missense_variant | MODERATE | c.508G>A|p.Glu170Lys |
S33 |