Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26590 | A02 | 14863502 | C | T | downstream_gene_variant | MODIFIER | c.*1227G>A| |
S206 |
2 | BAA02g26590 | A02 | 14863597 | G | A | downstream_gene_variant | MODIFIER | c.*1132C>T| |
S278 |
3 | BAA02g26590 | A02 | 14863801 | G | A | downstream_gene_variant | MODIFIER | c.*928C>T| |
S71 |
4 | BAA02g26590 | A02 | 14863849 | C | T | downstream_gene_variant | MODIFIER | c.*880G>A| |
S49 |
5 | BAA02g26590 | A02 | 14864042 | G | A | downstream_gene_variant | MODIFIER | c.*687C>T| |
S200 |
6 | BAA02g26590 | A02 | 14864952 | C | T | missense_variant | MODERATE | c.1541G>A|p.Gly514Glu |
S267 |
7 | BAA02g26590 | A02 | 14865191 | C | T | synonymous_variant | LOW | c.1302G>A|p.Gln434Gln |
S105 S106 |
8 | BAA02g26590 | A02 | 14865897 | G | A | missense_variant | MODERATE | c.596C>T|p.Pro199Leu |
S125 |
9 | BAA02g26590 | A02 | 14865989 | G | A | synonymous_variant | LOW | c.504C>T|p.Val168Val |
S68 |
10 | BAA02g26590 | A02 | 14867630 | G | A | upstream_gene_variant | MODIFIER | c.-1138C>T| |
S174 S27 |
11 | BAA02g26590 | A02 | 14868726 | G | A | upstream_gene_variant | MODIFIER | c.-2234C>T| |
S172 S202 |
12 | BAA02g26590 | A02 | 14870348 | G | A | upstream_gene_variant | MODIFIER | c.-3856C>T| |
S35 |