Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25300 | A02 | 13822511 | C | T | missense_variant | MODERATE | c.2386G>A|p.Glu796Lys |
S124 |
2 | BAA02g25300 | A02 | 13822704 | G | A | missense_variant | MODERATE | c.2260C>T|p.Pro754Ser |
S10 |
3 | BAA02g25300 | A02 | 13822968 | G | A | missense_variant | MODERATE | c.1996C>T|p.His666Tyr |
S187 |
4 | BAA02g25300 | A02 | 13822981 | G | A | synonymous_variant | LOW | c.1983C>T|p.Val661Val |
S163 |
5 | BAA02g25300 | A02 | 13823510 | C | T | missense_variant | MODERATE | c.1604G>A|p.Arg535Lys |
S82 |
6 | BAA02g25300 | A02 | 13823817 | G | A | stop_gained | HIGH | c.1459C>T|p.Gln487* |
S44 |
7 | BAA02g25300 | A02 | 13824329 | C | T | synonymous_variant | LOW | c.1092G>A|p.Lys364Lys |
S266 |
8 | BAA02g25300 | A02 | 13827208 | C | T | missense_variant | MODERATE | c.200G>A|p.Gly67Asp |
S118 |
9 | BAA02g25300 | A02 | 13827769 | C | T | upstream_gene_variant | MODIFIER | c.-129G>A| |
S9 |
10 | BAA02g25300 | A02 | 13828237 | G | A | upstream_gene_variant | MODIFIER | c.-597C>T| |
S130 S289 S290 |
11 | BAA02g25300 | A02 | 13829996 | G | A | upstream_gene_variant | MODIFIER | c.-2356C>T| |
S95 |
12 | BAA02g25300 | A02 | 13831727 | G | A | upstream_gene_variant | MODIFIER | c.-4087C>T| |
S237 |