Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46020 | A02 | 37525333 | G | A | upstream_gene_variant | MODIFIER | c.-4693G>A| |
S150 |
2 | BAA02g46020 | A02 | 37525547 | C | T | upstream_gene_variant | MODIFIER | c.-4479C>T| |
S305 |
3 | BAA02g46020 | A02 | 37526238 | C | T | upstream_gene_variant | MODIFIER | c.-3788C>T| |
S124 |
4 | BAA02g46020 | A02 | 37527226 | G | A | upstream_gene_variant | MODIFIER | c.-2800G>A| |
S197 |
5 | BAA02g46020 | A02 | 37528657 | G | A | upstream_gene_variant | MODIFIER | c.-1369G>A| |
S37 |
6 | BAA02g46020 | A02 | 37528737 | C | T | upstream_gene_variant | MODIFIER | c.-1289C>T| |
S95 |
7 | BAA02g46020 | A02 | 37528889 | C | T | upstream_gene_variant | MODIFIER | c.-1137C>T| |
S181 |
8 | BAA02g46020 | A02 | 37529351 | C | T | upstream_gene_variant | MODIFIER | c.-675C>T| |
S98 |
9 | BAA02g46020 | A02 | 37529573 | G | A | upstream_gene_variant | MODIFIER | c.-453G>A| |
S176 |
10 | BAA02g46020 | A02 | 37529946 | G | A | upstream_gene_variant | MODIFIER | c.-80G>A| |
S168 |
11 | BAA02g46020 | A02 | 37530119 | C | T | missense_variant | MODERATE | c.94C>T|p.Arg32Cys |
S32 |
12 | BAA02g46020 | A02 | 37535801 | G | A | downstream_gene_variant | MODIFIER | c.*4279G>A| |
S292 |
13 | BAA02g46020 | A02 | 37535933 | G | A | downstream_gene_variant | MODIFIER | c.*4411G>A| |
S62 |