Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12830 | A02 | 5747214 | C | T | synonymous_variant | LOW | c.2097G>A|p.Thr699Thr |
S212 |
2 | BAA02g12830 | A02 | 5747545 | G | A | missense_variant | MODERATE | c.1766C>T|p.Ser589Phe |
S187 |
3 | BAA02g12830 | A02 | 5748291 | C | T | missense_variant | MODERATE | c.1186G>A|p.Glu396Lys |
S75 |
4 | BAA02g12830 | A02 | 5749000 | C | T | missense_variant | MODERATE | c.647G>A|p.Arg216Lys |
S263 |
5 | BAA02g12830 | A02 | 5749168 | C | T | missense_variant | MODERATE | c.560G>A|p.Arg187Lys |
S242 |
6 | BAA02g12830 | A02 | 5749523 | G | A | missense_variant | MODERATE | c.205C>T|p.Leu69Phe |
S60 |
7 | BAA02g12830 | A02 | 5749676 | G | A | synonymous_variant | LOW | c.52C>T|p.Leu18Leu |
S164 |
8 | BAA02g12830 | A02 | 5750529 | C | T | upstream_gene_variant | MODIFIER | c.-715G>A| |
S13 |
9 | BAA02g12830 | A02 | 5750611 | C | T | upstream_gene_variant | MODIFIER | c.-797G>A| |
S266 |
10 | BAA02g12830 | A02 | 5751689 | C | T | upstream_gene_variant | MODIFIER | c.-1875G>A| |
S32 |
11 | BAA02g12830 | A02 | 5752488 | C | T | upstream_gene_variant | MODIFIER | c.-2674G>A| |
S306 S308 |
12 | BAA02g12830 | A02 | 5753230 | C | T | upstream_gene_variant | MODIFIER | c.-3416G>A| |
S266 |
13 | BAA02g12830 | A02 | 5753391 | C | T | upstream_gene_variant | MODIFIER | c.-3577G>A| |
S78 S83 |
14 | BAA02g12830 | A02 | 5753661 | C | T | upstream_gene_variant | MODIFIER | c.-3847G>A| |
S158 |
15 | BAA02g12830 | A02 | 5753915 | C | T | upstream_gene_variant | MODIFIER | c.-4101G>A| |
S172 S217 |