Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17750 | A01 | 8621030 | G | A | missense_variant | MODERATE | c.1673C>T|p.Ala558Val |
S34 |
2 | BAA01g17750 | A01 | 8621072 | C | T | missense_variant | MODERATE | c.1631G>A|p.Arg544Lys |
S184 |
3 | BAA01g17750 | A01 | 8621477 | C | T | missense_variant | MODERATE | c.1226G>A|p.Arg409Gln |
S176 |
4 | BAA01g17750 | A01 | 8621479 | G | A | synonymous_variant | LOW | c.1224C>T|p.Asn408Asn |
S294 |
5 | BAA01g17750 | A01 | 8621516 | G | A | missense_variant | MODERATE | c.1187C>T|p.Ala396Val |
S32 |
6 | BAA01g17750 | A01 | 8622108 | C | T | missense_variant | MODERATE | c.595G>A|p.Glu199Lys |
S231 |
7 | BAA01g17750 | A01 | 8622206 | C | T | missense_variant | MODERATE | c.497G>A|p.Arg166Gln |
S198 |
8 | BAA01g17750 | A01 | 8622324 | G | A | missense_variant | MODERATE | c.379C>T|p.Pro127Ser |
S9 |
9 | BAA01g17750 | A01 | 8622345 | C | T | missense_variant | MODERATE | c.358G>A|p.Glu120Lys |
S295 |
10 | BAA01g17750 | A01 | 8623699 | C | T | upstream_gene_variant | MODIFIER | c.-997G>A| |
S52 |
11 | BAA01g17750 | A01 | 8625306 | C | T | upstream_gene_variant | MODIFIER | c.-2604G>A| |
S259 |
12 | BAA01g17750 | A01 | 8625344 | G | A | upstream_gene_variant | MODIFIER | c.-2642C>T| |
S239 |
13 | BAA01g17750 | A01 | 8625730 | G | T | upstream_gene_variant | MODIFIER | c.-3028C>A| |
S226 |
14 | BAA01g17750 | A01 | 8626829 | C | T | upstream_gene_variant | MODIFIER | c.-4127G>A| |
S70 |