Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11690 | A02 | 5283642 | C | T | missense_variant | MODERATE | c.2929G>A|p.Asp977Asn |
S13 |
2 | BAA02g11690 | A02 | 5283802 | G | A | missense_variant | MODERATE | c.2867C>T|p.Ala956Val |
S286 |
3 | BAA02g11690 | A02 | 5283816 | C | T | synonymous_variant | LOW | c.2853G>A|p.Glu951Glu |
S115 |
4 | BAA02g11690 | A02 | 5284077 | C | T | missense_variant | MODERATE | c.2678G>A|p.Arg893His |
S199 |
5 | BAA02g11690 | A02 | 5287193 | C | T | intron_variant | MODIFIER | c.2515-2873G>A| |
S206 |
6 | BAA02g11690 | A02 | 5291764 | C | T | missense_variant | MODERATE | c.2411G>A|p.Gly804Glu |
S55 |
7 | BAA02g11690 | A02 | 5293389 | G | A | missense_variant | MODERATE | c.1369C>T|p.Leu457Phe |
S205 |
8 | BAA02g11690 | A02 | 5299178 | C | T | upstream_gene_variant | MODIFIER | c.-2832G>A| |
S103 |