Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21440 | A02 | 11534040 | C | T | upstream_gene_variant | MODIFIER | c.-4528C>T| |
S216 |
2 | BAA02g21440 | A02 | 11534230 | G | A | upstream_gene_variant | MODIFIER | c.-4338G>A| |
S109 |
3 | BAA02g21440 | A02 | 11534242 | C | T | upstream_gene_variant | MODIFIER | c.-4326C>T| |
S142 |
4 | BAA02g21440 | A02 | 11534960 | C | T | upstream_gene_variant | MODIFIER | c.-3608C>T| |
S97 |
5 | BAA02g21440 | A02 | 11536056 | C | T | upstream_gene_variant | MODIFIER | c.-2512C>T| |
S83 |
6 | BAA02g21440 | A02 | 11537063 | G | A | upstream_gene_variant | MODIFIER | c.-1505G>A| |
S202 |
7 | BAA02g21440 | A02 | 11537259 | A | G | upstream_gene_variant | MODIFIER | c.-1309A>G| |
S174 S216 S27 |
8 | BAA02g21440 | A02 | 11538558 | G | A | upstream_gene_variant | MODIFIER | c.-10G>A| |
S200 |
9 | BAA02g21440 | A02 | 11540405 | C | T | missense_variant | MODERATE | c.397C>T|p.Arg133Trp |
S293 |