Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40870 | A02 | 34277473 | G | A | downstream_gene_variant | MODIFIER | c.*4551C>T| |
S279 |
2 | BAA02g40870 | A02 | 34282100 | C | T | missense_variant | MODERATE | c.1259G>A|p.Gly420Asp |
S190 |
3 | BAA02g40870 | A02 | 34282290 | C | T | missense_variant | MODERATE | c.1069G>A|p.Ala357Thr |
S32 |
4 | BAA02g40870 | A02 | 34282342 | C | T | synonymous_variant | LOW | c.1017G>A|p.Ala339Ala |
S123 |
5 | BAA02g40870 | A02 | 34282366 | C | T | synonymous_variant | LOW | c.993G>A|p.Ser331Ser |
S105 S106 |
6 | BAA02g40870 | A02 | 34282480 | C | T | synonymous_variant | LOW | c.879G>A|p.Arg293Arg |
S68 |
7 | BAA02g40870 | A02 | 34283111 | G | A | missense_variant | MODERATE | c.248C>T|p.Pro83Leu |
S196 |
8 | BAA02g40870 | A02 | 34283116 | C | T | stop_gained | HIGH | c.243G>A|p.Trp81* |
S135 |
9 | BAA02g40870 | A02 | 34283209 | G | A | synonymous_variant | LOW | c.150C>T|p.His50His |
S199 |