Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g05990 | A03 | 2546096 | C | T | missense_variant | MODERATE | c.2198G>A|p.Gly733Asp |
S159 S243 |
2 | BAA03g05990 | A03 | 2546671 | C | T | missense_variant&splice_region_variant | MODERATE | c.1795G>A|p.Gly599Arg |
S42 |
3 | BAA03g05990 | A03 | 2547436 | G | A | missense_variant | MODERATE | c.1351C>T|p.Arg451Trp |
S1 S90 |
4 | BAA03g05990 | A03 | 2548365 | C | T | missense_variant | MODERATE | c.727G>A|p.Glu243Lys |
S193 |
5 | BAA03g05990 | A03 | 2549694 | G | A | intron_variant | MODIFIER | c.294+25C>T| |
S64 |
6 | BAA03g05990 | A03 | 2550162 | C | T | synonymous_variant | LOW | c.63G>A|p.Glu21Glu |
S195 |
7 | BAA03g05990 | A03 | 2550781 | C | T | upstream_gene_variant | MODIFIER | c.-132G>A| |
S263 |
8 | BAA03g05990 | A03 | 2550944 | G | A | upstream_gene_variant | MODIFIER | c.-295C>T| |
S36 |
9 | BAA03g05990 | A03 | 2551414 | G | A | upstream_gene_variant | MODIFIER | c.-765C>T| |
S162 |
10 | BAA03g05990 | A03 | 2551605 | C | T | upstream_gene_variant | MODIFIER | c.-956G>A| |
S225 |
11 | BAA03g05990 | A03 | 2551905 | C | T | upstream_gene_variant | MODIFIER | c.-1256G>A| |
S159 S243 S299 |
12 | BAA03g05990 | A03 | 2552341 | G | A | upstream_gene_variant | MODIFIER | c.-1692C>T| |
S94 |
13 | BAA03g05990 | A03 | 2553538 | C | T | upstream_gene_variant | MODIFIER | c.-2889G>A| |
S16 |
14 | BAA03g05990 | A03 | 2553830 | A | T | upstream_gene_variant | MODIFIER | c.-3181T>A| |
S272 |
15 | BAA03g05990 | A03 | 2554019 | A | T | upstream_gene_variant | MODIFIER | c.-3370T>A| |
S206 |
16 | BAA03g05990 | A03 | 2554938 | C | T | upstream_gene_variant | MODIFIER | c.-4289G>A| |
S208 S219 |