Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g38730 | A01 | 25830393 | C | T | missense_variant | MODERATE | c.2368G>A|p.Val790Ile |
S182 |
2 | BAA01g38730 | A01 | 25830916 | A | C | missense_variant | MODERATE | c.2070T>G|p.Phe690Leu |
S26 |
3 | BAA01g38730 | A01 | 25831429 | G | A | missense_variant | MODERATE | c.1625C>T|p.Ala542Val |
S159 S243 |
4 | BAA01g38730 | A01 | 25834046 | C | T | synonymous_variant | LOW | c.126G>A|p.Leu42Leu |
S62 |
5 | BAA01g38730 | A01 | 25834062 | G | A | missense_variant | MODERATE | c.110C>T|p.Pro37Leu |
S158 |
6 | BAA01g38730 | A01 | 25834283 | C | T | upstream_gene_variant | MODIFIER | c.-112G>A| |
S221 |
7 | BAA01g38730 | A01 | 25835926 | C | T | upstream_gene_variant | MODIFIER | c.-1755G>A| |
S289 S290 |
8 | BAA01g38730 | A01 | 25837206 | G | A | upstream_gene_variant | MODIFIER | c.-3035C>T| |
S36 |