Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g07960 | A05 | 3978940 | G | A | upstream_gene_variant | MODIFIER | c.-1316G>A| |
S306 S308 |
2 | BAA05g07960 | A05 | 3978986 | C | T | upstream_gene_variant | MODIFIER | c.-1270C>T| |
S72 S78 |
3 | BAA05g07960 | A05 | 3979397 | G | A | upstream_gene_variant | MODIFIER | c.-859G>A| |
S133 |
4 | BAA05g07960 | A05 | 3979422 | G | A | upstream_gene_variant | MODIFIER | c.-834G>A| |
S131 |
5 | BAA05g07960 | A05 | 3979905 | G | A | upstream_gene_variant | MODIFIER | c.-351G>A| |
S104 S52 |
6 | BAA05g07960 | A05 | 3980978 | G | A | missense_variant | MODERATE | c.497G>A|p.Gly166Glu |
S226 |
7 | BAA05g07960 | A05 | 3982125 | G | A | missense_variant | MODERATE | c.994G>A|p.Ala332Thr |
S161 |
8 | BAA05g07960 | A05 | 3982139 | G | A | synonymous_variant | LOW | c.1008G>A|p.Gln336Gln |
S46 |
9 | BAA05g07960 | A05 | 3982642 | C | T | missense_variant | MODERATE | c.1511C>T|p.Pro504Leu |
S235 |