Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15800 | A04 | 20463247 | C | T | downstream_gene_variant | MODIFIER | c.*2476G>A| |
S225 S73 |
2 | BAA04g15800 | A04 | 20465957 | G | A | synonymous_variant | LOW | c.2295C>T|p.Asn765Asn |
S186 |
3 | BAA04g15800 | A04 | 20466277 | C | T | missense_variant | MODERATE | c.1975G>A|p.Gly659Ser |
S242 |
4 | BAA04g15800 | A04 | 20466447 | G | A | missense_variant | MODERATE | c.1805C>T|p.Ala602Val |
S97 |
5 | BAA04g15800 | A04 | 20466647 | C | T | synonymous_variant | LOW | c.1605G>A|p.Thr535Thr |
S18 |
6 | BAA04g15800 | A04 | 20467122 | G | A | missense_variant | MODERATE | c.1130C>T|p.Thr377Ile |
S79 S91 |
7 | BAA04g15800 | A04 | 20468685 | G | A | upstream_gene_variant | MODIFIER | c.-315C>T| |
S156 |
8 | BAA04g15800 | A04 | 20468750 | C | T | upstream_gene_variant | MODIFIER | c.-380G>A| |
S200 S261 S303 |
9 | BAA04g15800 | A04 | 20470019 | G | A | upstream_gene_variant | MODIFIER | c.-1649C>T| |
S120 |
10 | BAA04g15800 | A04 | 20472410 | G | A | upstream_gene_variant | MODIFIER | c.-4040C>T| |
S50 |