Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15710 | A02 | 7604761 | C | T | upstream_gene_variant | MODIFIER | c.-1963C>T| |
S255 |
2 | BAA02g15710 | A02 | 7604769 | C | T | upstream_gene_variant | MODIFIER | c.-1955C>T| |
S262 |
3 | BAA02g15710 | A02 | 7605761 | C | T | upstream_gene_variant | MODIFIER | c.-963C>T| |
S128 |
4 | BAA02g15710 | A02 | 7605858 | C | T | upstream_gene_variant | MODIFIER | c.-866C>T| |
S18 |
5 | BAA02g15710 | A02 | 7605994 | G | A | upstream_gene_variant | MODIFIER | c.-730G>A| |
S166 |
6 | BAA02g15710 | A02 | 7606037 | G | A | upstream_gene_variant | MODIFIER | c.-687G>A| |
S188 |
7 | BAA02g15710 | A02 | 7606518 | G | A | upstream_gene_variant | MODIFIER | c.-206G>A| |
S19 |
8 | BAA02g15710 | A02 | 7606738 | G | A | synonymous_variant | LOW | c.15G>A|p.Gly5Gly |
S293 |
9 | BAA02g15710 | A02 | 7608784 | G | A | stop_gained | HIGH | c.978G>A|p.Trp326* |
S64 |
10 | BAA02g15710 | A02 | 7608891 | G | A | missense_variant | MODERATE | c.997G>A|p.Ala333Thr |
S169 |