Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21790 | A01 | 10843677 | G | A | upstream_gene_variant | MODIFIER | c.-3124G>A| |
S129 |
2 | BAA01g21790 | A01 | 10843778 | C | T | upstream_gene_variant | MODIFIER | c.-3023C>T| |
S87 |
3 | BAA01g21790 | A01 | 10846176 | G | A | upstream_gene_variant | MODIFIER | c.-625G>A| |
S149 |
4 | BAA01g21790 | A01 | 10846678 | C | T | upstream_gene_variant | MODIFIER | c.-123C>T| |
S259 |
5 | BAA01g21790 | A01 | 10847865 | G | A | missense_variant | MODERATE | c.760G>A|p.Glu254Lys |
S57 |
6 | BAA01g21790 | A01 | 10848023 | G | A | missense_variant | MODERATE | c.814G>A|p.Gly272Arg |
S149 |
7 | BAA01g21790 | A01 | 10848184 | G | A | missense_variant | MODERATE | c.902G>A|p.Gly301Glu |
S175 |
8 | BAA01g21790 | A01 | 10848226 | C | T | missense_variant | MODERATE | c.944C>T|p.Ala315Val |
S134 |
9 | BAA01g21790 | A01 | 10848900 | G | A | synonymous_variant | LOW | c.1347G>A|p.Leu449Leu |
S241 |