Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18660 | A02 | 9554813 | G | A | splice_region_variant&synonymous_variant | LOW | c.309C>T|p.His103His |
S116 |
2 | BAA02g18660 | A02 | 9555223 | T | G | intron_variant | MODIFIER | c.171+17A>C| |
S186 |
3 | BAA02g18660 | A02 | 9555256 | C | T | missense_variant | MODERATE | c.155G>A|p.Arg52Lys |
S105 S106 |
4 | BAA02g18660 | A02 | 9555905 | C | T | upstream_gene_variant | MODIFIER | c.-495G>A| |
S124 |
5 | BAA02g18660 | A02 | 9556731 | G | A | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S74 |
6 | BAA02g18660 | A02 | 9556789 | G | A | upstream_gene_variant | MODIFIER | c.-1379C>T| |
S223 |
7 | BAA02g18660 | A02 | 9557594 | T | C | upstream_gene_variant | MODIFIER | c.-2184A>G| |
S239 |
8 | BAA02g18660 | A02 | 9558059 | C | T | upstream_gene_variant | MODIFIER | c.-2649G>A| |
S249 |
9 | BAA02g18660 | A02 | 9558133 | C | T | upstream_gene_variant | MODIFIER | c.-2723G>A| |
S69 |
10 | BAA02g18660 | A02 | 9558192 | G | A | upstream_gene_variant | MODIFIER | c.-2782C>T| |
S28 |
11 | BAA02g18660 | A02 | 9558384 | G | A | upstream_gene_variant | MODIFIER | c.-2974C>T| |
S184 |
12 | BAA02g18660 | A02 | 9558549 | G | A | upstream_gene_variant | MODIFIER | c.-3139C>T| |
S43 |
13 | BAA02g18660 | A02 | 9558591 | C | T | upstream_gene_variant | MODIFIER | c.-3181G>A| |
S63 |
14 | BAA02g18660 | A02 | 9558630 | G | A | upstream_gene_variant | MODIFIER | c.-3220C>T| |
S162 |
15 | BAA02g18660 | A02 | 9558719 | C | T | upstream_gene_variant | MODIFIER | c.-3309G>A| |
S25 |
16 | BAA02g18660 | A02 | 9559354 | C | T | upstream_gene_variant | MODIFIER | c.-3944G>A| |
S46 |
17 | BAA02g18660 | A02 | 9559865 | C | T | upstream_gene_variant | MODIFIER | c.-4455G>A| |
S234 |