Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41770 | A05 | 39755538 | G | A | upstream_gene_variant | MODIFIER | c.-3912G>A| |
S125 |
2 | BAA05g41770 | A05 | 39755707 | G | A | upstream_gene_variant | MODIFIER | c.-3743G>A| |
S209 |
3 | BAA05g41770 | A05 | 39757509 | C | T | upstream_gene_variant | MODIFIER | c.-1941C>T| |
S197 |
4 | BAA05g41770 | A05 | 39758161 | G | A | upstream_gene_variant | MODIFIER | c.-1289G>A| |
S187 |
5 | BAA05g41770 | A05 | 39758171 | C | T | upstream_gene_variant | MODIFIER | c.-1279C>T| |
S282 |
6 | BAA05g41770 | A05 | 39758665 | C | T | upstream_gene_variant | MODIFIER | c.-785C>T| |
S54 |
7 | BAA05g41770 | A05 | 39759175 | C | T | upstream_gene_variant | MODIFIER | c.-275C>T| |
S117 |
8 | BAA05g41770 | A05 | 39759496 | G | A | missense_variant | MODERATE | c.47G>A|p.Gly16Glu |
S234 |
9 | BAA05g41770 | A05 | 39759506 | C | T | synonymous_variant | LOW | c.57C>T|p.Arg19Arg |
S192 |
10 | BAA05g41770 | A05 | 39763012 | C | T | downstream_gene_variant | MODIFIER | c.*2516C>T| |
S138 |
11 | BAA05g41770 | A05 | 39763401 | C | T | downstream_gene_variant | MODIFIER | c.*2905C>T| |
S257 |
12 | BAA05g41770 | A05 | 39764791 | G | A | downstream_gene_variant | MODIFIER | c.*4295G>A| |
S176 |