Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g09950 | A03 | 4093490 | C | T | missense_variant | MODERATE | c.472G>A|p.Ala158Thr |
S278 |
2 | BAA03g09950 | A03 | 4093666 | G | A | missense_variant | MODERATE | c.296C>T|p.Ala99Val |
S229 |
3 | BAA03g09950 | A03 | 4098869 | G | A | upstream_gene_variant | MODIFIER | c.-237C>T| |
S178 |
4 | BAA03g09950 | A03 | 4099471 | G | A | upstream_gene_variant | MODIFIER | c.-839C>T| |
S139 |
5 | BAA03g09950 | A03 | 4099863 | G | A | upstream_gene_variant | MODIFIER | c.-1231C>T| |
S165 |
6 | BAA03g09950 | A03 | 4100117 | G | A | upstream_gene_variant | MODIFIER | c.-1485C>T| |
S56 |
7 | BAA03g09950 | A03 | 4100256 | G | A | upstream_gene_variant | MODIFIER | c.-1624C>T| |
S56 |
8 | BAA03g09950 | A03 | 4100831 | G | T | upstream_gene_variant | MODIFIER | c.-2199C>A| |
S210 |
9 | BAA03g09950 | A03 | 4102538 | C | T | upstream_gene_variant | MODIFIER | c.-3906G>A| |
S38 |
10 | BAA03g09950 | A03 | 4102563 | G | A | upstream_gene_variant | MODIFIER | c.-3931C>T| |
S281 |
11 | BAA03g09950 | A03 | 4102593 | C | T | upstream_gene_variant | MODIFIER | c.-3961G>A| |
S144 |