Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40950 | A02 | 34330456 | C | T | missense_variant | MODERATE | c.1699G>A|p.Glu567Lys |
S133 |
2 | BAA02g40950 | A02 | 34331628 | C | T | intron_variant | MODIFIER | c.1123+141G>A| |
S210 |
3 | BAA02g40950 | A02 | 34332027 | C | T | intron_variant | MODIFIER | c.905-40G>A| |
S263 |
4 | BAA02g40950 | A02 | 34332954 | C | T | splice_region_variant&synonymous_variant | LOW | c.903G>A|p.Gln301Gln |
S63 |
5 | BAA02g40950 | A02 | 34334786 | G | A | upstream_gene_variant | MODIFIER | c.-930C>T| |
S302 |