Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00140 | A04 | 47399 | C | T | missense_variant | MODERATE | c.161C>T|p.Ser54Phe |
S194 |
2 | BAA04g00140 | A04 | 47872 | G | A | missense_variant | MODERATE | c.467G>A|p.Gly156Glu |
S60 |
3 | BAA04g00140 | A04 | 48388 | C | T | synonymous_variant | LOW | c.784C>T|p.Leu262Leu |
S281 S282 |
4 | BAA04g00140 | A04 | 48693 | C | T | missense_variant | MODERATE | c.1003C>T|p.Pro335Ser |
S170 S176 |
5 | BAA04g00140 | A04 | 52219 | G | A | downstream_gene_variant | MODIFIER | c.*3407G>A| |
S171 |