Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66780 | A03 | 41273540 | G | A | downstream_gene_variant | MODIFIER | c.*195C>T| |
S197 |
2 | BAA03g66780 | A03 | 41274742 | G | A | splice_region_variant&synonymous_variant | LOW | c.288C>T|p.Arg96Arg |
S286 |
3 | BAA03g66780 | A03 | 41275036 | C | T | intron_variant | MODIFIER | c.226-232G>A| |
S257 |
4 | BAA03g66780 | A03 | 41275255 | G | A | intron_variant | MODIFIER | c.226-451C>T| |
S286 |
5 | BAA03g66780 | A03 | 41275914 | C | T | missense_variant | MODERATE | c.151G>A|p.Ala51Thr |
S105 S106 |
6 | BAA03g66780 | A03 | 41275931 | G | A | missense_variant | MODERATE | c.134C>T|p.Pro45Leu |
S218 |
7 | BAA03g66780 | A03 | 41275973 | T | G | missense_variant | MODERATE | c.92A>C|p.Lys31Thr |
S276 |
8 | BAA03g66780 | A03 | 41277490 | C | T | upstream_gene_variant | MODIFIER | c.-1352G>A| |
S153 |
9 | BAA03g66780 | A03 | 41277973 | C | T | upstream_gene_variant | MODIFIER | c.-1835G>A| |
S232 |
10 | BAA03g66780 | A03 | 41277996 | C | T | upstream_gene_variant | MODIFIER | c.-1858G>A| |
S113 |
11 | BAA03g66780 | A03 | 41278045 | C | T | upstream_gene_variant | MODIFIER | c.-1907G>A| |
S4 |
12 | BAA03g66780 | A03 | 41278246 | G | A | upstream_gene_variant | MODIFIER | c.-2108C>T| |
S186 |
13 | BAA03g66780 | A03 | 41278673 | C | T | upstream_gene_variant | MODIFIER | c.-2535G>A| |
S163 |
14 | BAA03g66780 | A03 | 41278801 | G | A | upstream_gene_variant | MODIFIER | c.-2663C>T| |
S183 S198 |
15 | BAA03g66780 | A03 | 41278909 | G | A | upstream_gene_variant | MODIFIER | c.-2771C>T| |
S168 |
16 | BAA03g66780 | A03 | 41279039 | C | T | upstream_gene_variant | MODIFIER | c.-2901G>A| |
S134 |
17 | BAA03g66780 | A03 | 41279379 | G | A | upstream_gene_variant | MODIFIER | c.-3241C>T| |
S294 |