Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g11960 | A04 | 17851248 | G | A | upstream_gene_variant | MODIFIER | c.-2806G>A| |
S136 |
2 | BAA04g11960 | A04 | 17851366 | G | A | upstream_gene_variant | MODIFIER | c.-2688G>A| |
S116 |
3 | BAA04g11960 | A04 | 17852244 | C | T | upstream_gene_variant | MODIFIER | c.-1810C>T| |
S296 |
4 | BAA04g11960 | A04 | 17852805 | G | A | upstream_gene_variant | MODIFIER | c.-1249G>A| |
S69 |
5 | BAA04g11960 | A04 | 17853568 | G | A | upstream_gene_variant | MODIFIER | c.-486G>A| |
S205 |
6 | BAA04g11960 | A04 | 17853668 | C | T | upstream_gene_variant | MODIFIER | c.-386C>T| |
S107 |
7 | BAA04g11960 | A04 | 17854200 | G | A | synonymous_variant | LOW | c.147G>A|p.Glu49Glu |
S138 |
8 | BAA04g11960 | A04 | 17855066 | C | T | missense_variant | MODERATE | c.1013C>T|p.Ser338Phe |
S202 |
9 | BAA04g11960 | A04 | 17855077 | G | A | missense_variant | MODERATE | c.1024G>A|p.Ala342Thr |
S308 |