Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18000 | A02 | 9041812 | G | A | downstream_gene_variant | MODIFIER | c.*1738C>T| |
S174 S27 |
2 | BAA02g18000 | A02 | 9041831 | C | T | downstream_gene_variant | MODIFIER | c.*1719G>A| |
S290 |
3 | BAA02g18000 | A02 | 9043507 | C | T | downstream_gene_variant | MODIFIER | c.*43G>A| |
S266 |
4 | BAA02g18000 | A02 | 9043801 | C | T | missense_variant | MODERATE | c.1390G>A|p.Val464Ile |
S221 |
5 | BAA02g18000 | A02 | 9043930 | C | T | missense_variant | MODERATE | c.1261G>A|p.Asp421Asn |
S270 |
6 | BAA02g18000 | A02 | 9045540 | C | T | missense_variant | MODERATE | c.230G>A|p.Gly77Glu |
S75 S81 |
7 | BAA02g18000 | A02 | 9045563 | G | A | synonymous_variant | LOW | c.207C>T|p.Pro69Pro |
S170 |
8 | BAA02g18000 | A02 | 9048033 | G | A | upstream_gene_variant | MODIFIER | c.-1359C>T| |
S188 |
9 | BAA02g18000 | A02 | 9048085 | G | A | upstream_gene_variant | MODIFIER | c.-1411C>T| |
S19 |
10 | BAA02g18000 | A02 | 9048789 | C | T | upstream_gene_variant | MODIFIER | c.-2115G>A| |
S166 |
11 | BAA02g18000 | A02 | 9049475 | C | A | upstream_gene_variant | MODIFIER | c.-2801G>T| |
S77 S82 |