Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39770 | A01 | 26423981 | C | T | missense_variant | MODERATE | c.545C>T|p.Thr182Met |
S16 |
2 | BAA01g39770 | A01 | 26424541 | C | T | missense_variant | MODERATE | c.1105C>T|p.Pro369Ser |
S174 S27 |
3 | BAA01g39770 | A01 | 26424569 | G | A | missense_variant | MODERATE | c.1133G>A|p.Arg378Gln |
S39 |
4 | BAA01g39770 | A01 | 26425707 | G | A | downstream_gene_variant | MODIFIER | c.*987G>A| |
S250 |
5 | BAA01g39770 | A01 | 26425872 | G | A | downstream_gene_variant | MODIFIER | c.*1152G>A| |
S125 |