Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40960 | A01 | 27117328 | C | T | missense_variant | MODERATE | c.139C>T|p.Pro47Ser |
S246 |
2 | BAA01g40960 | A01 | 27117384 | C | T | synonymous_variant | LOW | c.195C>T|p.Phe65Phe |
S83 |
3 | BAA01g40960 | A01 | 27117502 | G | A | downstream_gene_variant | MODIFIER | c.*58G>A| |
S234 |
4 | BAA01g40960 | A01 | 27119556 | G | A | downstream_gene_variant | MODIFIER | c.*2112G>A| |
S184 |
5 | BAA01g40960 | A01 | 27120379 | C | T | downstream_gene_variant | MODIFIER | c.*2935C>T| |
S197 |