Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43940 | A02 | 36281615 | C | T | missense_variant | MODERATE | c.1405G>A|p.Asp469Asn |
S202 |
2 | BAA02g43940 | A02 | 36281772 | C | T | synonymous_variant | LOW | c.1248G>A|p.Glu416Glu |
S195 |
3 | BAA02g43940 | A02 | 36281859 | G | A | synonymous_variant | LOW | c.1161C>T|p.Ile387Ile |
S297 |
4 | BAA02g43940 | A02 | 36282111 | G | A | synonymous_variant | LOW | c.909C>T|p.Ala303Ala |
S50 |
5 | BAA02g43940 | A02 | 36282621 | G | A | missense_variant | MODERATE | c.479C>T|p.Ala160Val |
S113 |
6 | BAA02g43940 | A02 | 36282797 | G | A | synonymous_variant | LOW | c.303C>T|p.Tyr101Tyr |
S221 |
7 | BAA02g43940 | A02 | 36286634 | C | T | upstream_gene_variant | MODIFIER | c.-3535G>A| |
S174 |
8 | BAA02g43940 | A02 | 36287806 | G | A | upstream_gene_variant | MODIFIER | c.-4707C>T| |
S255 |