Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30980 | A02 | 18301941 | C | T | upstream_gene_variant | MODIFIER | c.-1750C>T| |
S138 |
2 | BAA02g30980 | A02 | 18303315 | G | A | upstream_gene_variant | MODIFIER | c.-376G>A| |
S174 |
3 | BAA02g30980 | A02 | 18303414 | C | T | upstream_gene_variant | MODIFIER | c.-277C>T| |
S296 |
4 | BAA02g30980 | A02 | 18303425 | G | A | upstream_gene_variant | MODIFIER | c.-266G>A| |
S17 |
5 | BAA02g30980 | A02 | 18303494 | C | T | upstream_gene_variant | MODIFIER | c.-197C>T| |
S135 |
6 | BAA02g30980 | A02 | 18303716 | C | T | missense_variant | MODERATE | c.26C>T|p.Ala9Val |
S211 |
7 | BAA02g30980 | A02 | 18304923 | G | A | missense_variant | MODERATE | c.482G>A|p.Gly161Glu |
S245 |
8 | BAA02g30980 | A02 | 18304980 | C | T | missense_variant | MODERATE | c.539C>T|p.Ser180Phe |
S165 |
9 | BAA02g30980 | A02 | 18305134 | G | A | missense_variant | MODERATE | c.613G>A|p.Glu205Lys |
S225 |
10 | BAA02g30980 | A02 | 18305192 | C | T | missense_variant | MODERATE | c.671C>T|p.Thr224Ile |
S75 S81 |
11 | BAA02g30980 | A02 | 18306918 | C | T | downstream_gene_variant | MODIFIER | c.*1689C>T| |
S177 |
12 | BAA02g30980 | A02 | 18307202 | C | T | downstream_gene_variant | MODIFIER | c.*1973C>T| |
S40 |
13 | BAA02g30980 | A02 | 18308810 | G | A | downstream_gene_variant | MODIFIER | c.*3581G>A| |
S56 |
14 | BAA02g30980 | A02 | 18309340 | C | T | downstream_gene_variant | MODIFIER | c.*4111C>T| |
S88 |
15 | BAA02g30980 | A02 | 18309781 | G | A | downstream_gene_variant | MODIFIER | c.*4552G>A| |
S186 |