Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g22380 | A03 | 10171822 | C | T | upstream_gene_variant | MODIFIER | c.-4695C>T| |
S42 |
2 | BAA03g22380 | A03 | 10173043 | C | T | upstream_gene_variant | MODIFIER | c.-3474C>T| |
S278 |
3 | BAA03g22380 | A03 | 10173263 | G | A | upstream_gene_variant | MODIFIER | c.-3254G>A| |
S162 |
4 | BAA03g22380 | A03 | 10174025 | G | A | upstream_gene_variant | MODIFIER | c.-2492G>A| |
S51 |
5 | BAA03g22380 | A03 | 10174529 | C | T | upstream_gene_variant | MODIFIER | c.-1988C>T| |
S144 |
6 | BAA03g22380 | A03 | 10176642 | C | T | synonymous_variant | LOW | c.126C>T|p.Ser42Ser |
S16 |
7 | BAA03g22380 | A03 | 10176788 | C | T | missense_variant | MODERATE | c.272C>T|p.Pro91Leu |
S259 |
8 | BAA03g22380 | A03 | 10176979 | G | A | missense_variant | MODERATE | c.463G>A|p.Val155Ile |
S149 |
9 | BAA03g22380 | A03 | 10178586 | C | T | synonymous_variant | LOW | c.1317C>T|p.Thr439Thr |
S265 |
10 | BAA03g22380 | A03 | 10178846 | C | T | missense_variant | MODERATE | c.1445C>T|p.Ser482Leu |
S112 |
11 | BAA03g22380 | A03 | 10178899 | G | A | missense_variant | MODERATE | c.1498G>A|p.Gly500Ser |
S294 |
12 | BAA03g22380 | A03 | 10179625 | C | T | synonymous_variant | LOW | c.2224C>T|p.Leu742Leu |
S159 S243 |
13 | BAA03g22380 | A03 | 10180039 | G | A | missense_variant | MODERATE | c.2638G>A|p.Val880Ile |
S267 |