Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10380 | A01 | 4745550 | C | T | missense_variant | MODERATE | c.881G>A|p.Gly294Glu |
S47 |
2 | BAA01g10380 | A01 | 4745679 | C | T | missense_variant | MODERATE | c.752G>A|p.Arg251Gln |
S166 |
3 | BAA01g10380 | A01 | 4746148 | C | T | missense_variant | MODERATE | c.283G>A|p.Ala95Thr |
S202 |
4 | BAA01g10380 | A01 | 4748210 | G | A | upstream_gene_variant | MODIFIER | c.-1780C>T| |
S281 |
5 | BAA01g10380 | A01 | 4748388 | C | T | upstream_gene_variant | MODIFIER | c.-1958G>A| |
S176 |
6 | BAA01g10380 | A01 | 4750118 | G | A | upstream_gene_variant | MODIFIER | c.-3688C>T| |
S69 |
7 | BAA01g10380 | A01 | 4750303 | C | T | upstream_gene_variant | MODIFIER | c.-3873G>A| |
S41 |