Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43280 | A02 | 35893293 | G | A | upstream_gene_variant | MODIFIER | c.-630G>A| |
S70 |
2 | BAA02g43280 | A02 | 35894513 | G | A | missense_variant | MODERATE | c.400G>A|p.Gly134Ser |
S213 |
3 | BAA02g43280 | A02 | 35894650 | G | A | synonymous_variant | LOW | c.537G>A|p.Gln179Gln |
S200 |
4 | BAA02g43280 | A02 | 35894762 | G | A | missense_variant | MODERATE | c.649G>A|p.Gly217Arg |
S209 |
5 | BAA02g43280 | A02 | 35895059 | C | T | missense_variant | MODERATE | c.946C>T|p.Pro316Ser |
S182 |
6 | BAA02g43280 | A02 | 35895401 | C | T | stop_gained | HIGH | c.1288C>T|p.Gln430* |
S95 |
7 | BAA02g43280 | A02 | 35895911 | G | A | missense_variant | MODERATE | c.1798G>A|p.Glu600Lys |
S134 |
8 | BAA02g43280 | A02 | 35896195 | C | T | synonymous_variant | LOW | c.2082C>T|p.Leu694Leu |
S252 |
9 | BAA02g43280 | A02 | 35898821 | C | T | downstream_gene_variant | MODIFIER | c.*2176C>T| |
S267 |
10 | BAA02g43280 | A02 | 35899366 | C | T | downstream_gene_variant | MODIFIER | c.*2721C>T| |
S269 |
11 | BAA02g43280 | A02 | 35899495 | C | T | downstream_gene_variant | MODIFIER | c.*2850C>T| |
S159 S243 |
12 | BAA02g43280 | A02 | 35899733 | C | T | downstream_gene_variant | MODIFIER | c.*3088C>T| |
S195 |
13 | BAA02g43280 | A02 | 35899760 | G | A | downstream_gene_variant | MODIFIER | c.*3115G>A| |
S148 S210 S31 |
14 | BAA02g43280 | A02 | 35900765 | G | A | downstream_gene_variant | MODIFIER | c.*4120G>A| |
S291 |
15 | BAA02g43280 | A02 | 35901150 | G | A | downstream_gene_variant | MODIFIER | c.*4505G>A| |
S192 |