Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20270 | A02 | 10686474 | G | A | missense_variant | MODERATE | c.8G>A|p.Arg3Lys |
S279 |
2 | BAA02g20270 | A02 | 10686562 | C | T | synonymous_variant | LOW | c.96C>T|p.Ser32Ser |
S302 |
3 | BAA02g20270 | A02 | 10686754 | C | T | synonymous_variant | LOW | c.288C>T|p.Val96Val |
S108 |
4 | BAA02g20270 | A02 | 10687602 | G | A | missense_variant | MODERATE | c.1136G>A|p.Arg379Lys |
S291 |
5 | BAA02g20270 | A02 | 10692067 | C | T | downstream_gene_variant | MODIFIER | c.*3750C>T| |
S6 |