Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45940 | A02 | 37485003 | G | A | downstream_gene_variant | MODIFIER | c.*1422C>T| |
S25 |
2 | BAA02g45940 | A02 | 37487066 | C | T | missense_variant | MODERATE | c.20G>A|p.Ser7Asn |
S135 |
3 | BAA02g45940 | A02 | 37487130 | G | A | upstream_gene_variant | MODIFIER | c.-45C>T| |
S156 |
4 | BAA02g45940 | A02 | 37487156 | C | T | upstream_gene_variant | MODIFIER | c.-71G>A| |
S19 |
5 | BAA02g45940 | A02 | 37488702 | C | T | upstream_gene_variant | MODIFIER | c.-1617G>A| |
S108 |
6 | BAA02g45940 | A02 | 37489597 | C | T | upstream_gene_variant | MODIFIER | c.-2512G>A| |
S4 |
7 | BAA02g45940 | A02 | 37489717 | C | T | upstream_gene_variant | MODIFIER | c.-2632G>A| |
S18 |
8 | BAA02g45940 | A02 | 37490013 | G | A | upstream_gene_variant | MODIFIER | c.-2928C>T| |
S205 |
9 | BAA02g45940 | A02 | 37490586 | C | T | upstream_gene_variant | MODIFIER | c.-3501G>A| |
S13 |
10 | BAA02g45940 | A02 | 37490873 | G | A | upstream_gene_variant | MODIFIER | c.-3788C>T| |
S127 |
11 | BAA02g45940 | A02 | 37492072 | G | A | upstream_gene_variant | MODIFIER | c.-4987C>T| |
S127 |