Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00250 | A02 | 145184 | C | T | upstream_gene_variant | MODIFIER | c.-4313C>T| |
S270 |
2 | BAA02g00250 | A02 | 146273 | G | A | upstream_gene_variant | MODIFIER | c.-3224G>A| |
S206 S26 |
3 | BAA02g00250 | A02 | 147997 | G | A | upstream_gene_variant | MODIFIER | c.-1500G>A| |
S90 |
4 | BAA02g00250 | A02 | 148556 | C | A | upstream_gene_variant | MODIFIER | c.-941C>A| |
S182 |
5 | BAA02g00250 | A02 | 149293 | G | A | upstream_gene_variant | MODIFIER | c.-204G>A| |
S20 |
6 | BAA02g00250 | A02 | 149669 | G | A | missense_variant | MODERATE | c.173G>A|p.Arg58Lys |
S60 |
7 | BAA02g00250 | A02 | 150777 | G | A | missense_variant | MODERATE | c.569G>A|p.Ser190Asn |
S128 |
8 | BAA02g00250 | A02 | 151019 | G | A | missense_variant | MODERATE | c.811G>A|p.Glu271Lys |
S302 |
9 | BAA02g00250 | A02 | 151028 | G | A | missense_variant | MODERATE | c.820G>A|p.Asp274Asn |
S189 |