Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05170 | A02 | 2272479 | C | T | upstream_gene_variant | MODIFIER | c.-805C>T| |
S108 |
2 | BAA02g05170 | A02 | 2273432 | C | T | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S298 |
3 | BAA02g05170 | A02 | 2273538 | C | T | synonymous_variant | LOW | c.255C>T|p.Leu85Leu |
S240 |
4 | BAA02g05170 | A02 | 2273607 | C | T | synonymous_variant | LOW | c.324C>T|p.Leu108Leu |
S230 |
5 | BAA02g05170 | A02 | 2273730 | G | A | stop_gained | HIGH | c.447G>A|p.Trp149* |
S293 |
6 | BAA02g05170 | A02 | 2273737 | C | T | missense_variant | MODERATE | c.454C>T|p.Leu152Phe |
S178 |
7 | BAA02g05170 | A02 | 2274307 | G | A | missense_variant | MODERATE | c.1024G>A|p.Val342Met |
S202 |
8 | BAA02g05170 | A02 | 2274398 | G | A | missense_variant | MODERATE | c.1115G>A|p.Gly372Asp |
S228 |
9 | BAA02g05170 | A02 | 2275545 | C | T | missense_variant | MODERATE | c.1817C>T|p.Ser606Phe |
S85 |
10 | BAA02g05170 | A02 | 2276069 | G | A | missense_variant | MODERATE | c.2233G>A|p.Val745Ile |
S275 |
11 | BAA02g05170 | A02 | 2276387 | G | A | missense_variant | MODERATE | c.2551G>A|p.Ala851Thr |
S107 |
12 | BAA02g05170 | A02 | 2276758 | G | A | synonymous_variant | LOW | c.2922G>A|p.Leu974Leu |
S271 |