Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20630 | A02 | 10928133 | C | T | upstream_gene_variant | MODIFIER | c.-4445C>T| |
S124 |
2 | BAA02g20630 | A02 | 10929361 | G | A | upstream_gene_variant | MODIFIER | c.-3217G>A| |
S264 |
3 | BAA02g20630 | A02 | 10929758 | G | A | upstream_gene_variant | MODIFIER | c.-2820G>A| |
S45 |
4 | BAA02g20630 | A02 | 10929761 | G | A | upstream_gene_variant | MODIFIER | c.-2817G>A| |
S36 |
5 | BAA02g20630 | A02 | 10929948 | C | T | upstream_gene_variant | MODIFIER | c.-2630C>T| |
S183 S198 |
6 | BAA02g20630 | A02 | 10931020 | G | A | upstream_gene_variant | MODIFIER | c.-1558G>A| |
S44 |
7 | BAA02g20630 | A02 | 10931134 | C | T | upstream_gene_variant | MODIFIER | c.-1444C>T| |
S233 |
8 | BAA02g20630 | A02 | 10932620 | G | A | splice_donor_variant&intron_variant | HIGH | c.42+1G>A| |
S287 |
9 | BAA02g20630 | A02 | 10932799 | G | A | missense_variant | MODERATE | c.133G>A|p.Ala45Thr |
S232 |
10 | BAA02g20630 | A02 | 10935484 | G | A | missense_variant | MODERATE | c.1721G>A|p.Gly574Glu |
S288 |
11 | BAA02g20630 | A02 | 10937041 | G | A | downstream_gene_variant | MODIFIER | c.*1508G>A| |
S223 |
12 | BAA02g20630 | A02 | 10937299 | C | T | downstream_gene_variant | MODIFIER | c.*1766C>T| |
S273 |