Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16660 | A01 | 8109857 | C | T | missense_variant | MODERATE | c.677G>A|p.Arg226Lys |
S47 |
2 | BAA01g16660 | A01 | 8110297 | C | T | missense_variant | MODERATE | c.562G>A|p.Ala188Thr |
S299 |
3 | BAA01g16660 | A01 | 8111086 | G | A | synonymous_variant | LOW | c.297C>T|p.Val99Val |
S94 |
4 | BAA01g16660 | A01 | 8111105 | C | T | missense_variant | MODERATE | c.278G>A|p.Gly93Glu |
S139 |
5 | BAA01g16660 | A01 | 8113784 | C | T | upstream_gene_variant | MODIFIER | c.-2402G>A| |
S146 |
6 | BAA01g16660 | A01 | 8115185 | G | A | upstream_gene_variant | MODIFIER | c.-3803C>T| |
S252 |
7 | BAA01g16660 | A01 | 8115580 | G | A | upstream_gene_variant | MODIFIER | c.-4198C>T| |
S163 |
8 | BAA01g16660 | A01 | 8116187 | G | A | upstream_gene_variant | MODIFIER | c.-4805C>T| |
S178 |