Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39850 | A01 | 26465160 | C | T | missense_variant | MODERATE | c.2077G>A|p.Glu693Lys |
S41 |
2 | BAA01g39850 | A01 | 26465688 | C | T | missense_variant | MODERATE | c.1549G>A|p.Ala517Thr |
S98 |
3 | BAA01g39850 | A01 | 26467129 | G | A | synonymous_variant | LOW | c.108C>T|p.Phe36Phe |
S238 |
4 | BAA01g39850 | A01 | 26467970 | C | T | upstream_gene_variant | MODIFIER | c.-734G>A| |
S7 |
5 | BAA01g39850 | A01 | 26469666 | G | A | upstream_gene_variant | MODIFIER | c.-2430C>T| |
S244 |
6 | BAA01g39850 | A01 | 26471210 | G | A | upstream_gene_variant | MODIFIER | c.-3974C>T| |
S232 |
7 | BAA01g39850 | A01 | 26471231 | G | A | upstream_gene_variant | MODIFIER | c.-3995C>T| |
S186 |
8 | BAA01g39850 | A01 | 26471500 | G | A | upstream_gene_variant | MODIFIER | c.-4264C>T| |
S286 |
9 | BAA01g39850 | A01 | 26471586 | G | A | upstream_gene_variant | MODIFIER | c.-4350C>T| |
S61 |