Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42760 | A02 | 35593464 | C | T | synonymous_variant | LOW | c.36C>T|p.Leu12Leu |
S242 |
2 | BAA02g42760 | A02 | 35594554 | C | T | missense_variant | MODERATE | c.298C>T|p.Leu100Phe |
S212 |
3 | BAA02g42760 | A02 | 35594599 | G | A | missense_variant&splice_region_variant | MODERATE | c.343G>A|p.Glu115Lys |
S191 |
4 | BAA02g42760 | A02 | 35595305 | G | A | synonymous_variant | LOW | c.585G>A|p.Arg195Arg |
S125 |
5 | BAA02g42760 | A02 | 35598329 | G | A | downstream_gene_variant | MODIFIER | c.*172G>A| |
S163 |
6 | BAA02g42760 | A02 | 35598351 | C | T | downstream_gene_variant | MODIFIER | c.*194C>T| |
S87 |
7 | BAA02g42760 | A02 | 35599928 | A | T | downstream_gene_variant | MODIFIER | c.*1771A>T| |
|
8 | BAA02g42760 | A02 | 35600839 | G | A | downstream_gene_variant | MODIFIER | c.*2682G>A| |
S13 |
9 | BAA02g42760 | A02 | 35602074 | C | T | downstream_gene_variant | MODIFIER | c.*3917C>T| |
S179 |
10 | BAA02g42760 | A02 | 35602262 | G | A | downstream_gene_variant | MODIFIER | c.*4105G>A| |
S89 |