Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00650 | A04 | 369606 | C | T | synonymous_variant | LOW | c.927G>A|p.Arg309Arg |
S140 |
2 | BAA04g00650 | A04 | 369831 | C | T | missense_variant | MODERATE | c.702G>A|p.Met234Ile |
S294 |
3 | BAA04g00650 | A04 | 369902 | G | A | missense_variant | MODERATE | c.631C>T|p.Pro211Ser |
S194 |
4 | BAA04g00650 | A04 | 369996 | C | T | synonymous_variant | LOW | c.537G>A|p.Lys179Lys |
S204 |
5 | BAA04g00650 | A04 | 370183 | C | T | missense_variant | MODERATE | c.350G>A|p.Ser117Asn |
S242 |
6 | BAA04g00650 | A04 | 370340 | C | T | missense_variant | MODERATE | c.193G>A|p.Ala65Thr |
S168 |
7 | BAA04g00650 | A04 | 374830 | C | T | upstream_gene_variant | MODIFIER | c.-4298G>A| |
S130 |
8 | BAA04g00650 | A04 | 375026 | G | A | upstream_gene_variant | MODIFIER | c.-4494C>T| |
S78 |