Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38020 | A09 | 46054866 | G | A | missense_variant | MODERATE | c.521C>T|p.Ala174Val |
S203 |
2 | BAA09g38020 | A09 | 46058352 | C | T | intron_variant | MODIFIER | c.358+1447G>A| |
S213 |
3 | BAA09g38020 | A09 | 46059651 | C | T | intron_variant | MODIFIER | c.358+148G>A| |
S109 |
4 | BAA09g38020 | A09 | 46059974 | C | T | synonymous_variant | LOW | c.183G>A|p.Lys61Lys |
S296 |
5 | BAA09g38020 | A09 | 46061366 | G | A | upstream_gene_variant | MODIFIER | c.-1210C>T| |
S4 |
6 | BAA09g38020 | A09 | 46062450 | C | T | upstream_gene_variant | MODIFIER | c.-2294G>A| |
S195 |
7 | BAA09g38020 | A09 | 46062824 | G | A | upstream_gene_variant | MODIFIER | c.-2668C>T| |
S271 |