Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g33370 | A02 | 28587035 | C | T | upstream_gene_variant | MODIFIER | c.-3531C>T| |
S202 |
2 | BAA02g33370 | A02 | 28587213 | G | A | upstream_gene_variant | MODIFIER | c.-3353G>A| |
S247 |
3 | BAA02g33370 | A02 | 28588375 | G | A | upstream_gene_variant | MODIFIER | c.-2191G>A| |
S186 |
4 | BAA02g33370 | A02 | 28588520 | C | T | upstream_gene_variant | MODIFIER | c.-2046C>T| |
S201 |
5 | BAA02g33370 | A02 | 28589857 | G | A | upstream_gene_variant | MODIFIER | c.-709G>A| |
S127 |
6 | BAA02g33370 | A02 | 28590863 | G | A | missense_variant | MODERATE | c.298G>A|p.Val100Met |
S148 S210 S30 S31 |
7 | BAA02g33370 | A02 | 28591884 | G | A | missense_variant | MODERATE | c.430G>A|p.Gly144Arg |
S67 |
8 | BAA02g33370 | A02 | 28591886 | G | A | synonymous_variant | LOW | c.432G>A|p.Gly144Gly |
S80 |
9 | BAA02g33370 | A02 | 28592069 | C | T | intron_variant | MODIFIER | c.516+99C>T| |
S179 |
10 | BAA02g33370 | A02 | 28592420 | C | T | missense_variant | MODERATE | c.755C>T|p.Thr252Ile |
S64 |
11 | BAA02g33370 | A02 | 28592655 | G | A | missense_variant | MODERATE | c.910G>A|p.Gly304Ser |
S62 |
12 | BAA02g33370 | A02 | 28594426 | C | T | downstream_gene_variant | MODIFIER | c.*1376C>T| |
S130 |