Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20070 | A02 | 10571646 | G | A | upstream_gene_variant | MODIFIER | c.-3620G>A| |
S60 |
2 | BAA02g20070 | A02 | 10572558 | C | T | upstream_gene_variant | MODIFIER | c.-2708C>T| |
S123 |
3 | BAA02g20070 | A02 | 10572642 | G | A | upstream_gene_variant | MODIFIER | c.-2624G>A| |
S67 |
4 | BAA02g20070 | A02 | 10572689 | C | T | upstream_gene_variant | MODIFIER | c.-2577C>T| |
S182 |
5 | BAA02g20070 | A02 | 10574280 | G | A | upstream_gene_variant | MODIFIER | c.-986G>A| |
S47 |
6 | BAA02g20070 | A02 | 10575103 | G | A | upstream_gene_variant | MODIFIER | c.-163G>A| |
S263 |
7 | BAA02g20070 | A02 | 10575147 | C | T | upstream_gene_variant | MODIFIER | c.-119C>T| |
S267 |
8 | BAA02g20070 | A02 | 10576199 | C | T | missense_variant | MODERATE | c.260C>T|p.Thr87Ile |
S290 |
9 | BAA02g20070 | A02 | 10577621 | C | T | downstream_gene_variant | MODIFIER | c.*67C>T| |
S114 |
10 | BAA02g20070 | A02 | 10579620 | C | T | downstream_gene_variant | MODIFIER | c.*2066C>T| |
S242 |
11 | BAA02g20070 | A02 | 10579990 | C | T | downstream_gene_variant | MODIFIER | c.*2436C>T| |
S177 |
12 | BAA02g20070 | A02 | 10580600 | C | T | downstream_gene_variant | MODIFIER | c.*3046C>T| |
S178 |
13 | BAA02g20070 | A02 | 10581709 | G | A | downstream_gene_variant | MODIFIER | c.*4155G>A| |
S152 |