Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10120 | A02 | 4479099 | C | T | missense_variant | MODERATE | c.622G>A|p.Asp208Asn |
S123 |
2 | BAA02g10120 | A02 | 4479346 | C | T | synonymous_variant | LOW | c.375G>A|p.Glu125Glu |
S94 |
3 | BAA02g10120 | A02 | 4479373 | C | T | synonymous_variant | LOW | c.348G>A|p.Gly116Gly |
S2 |
4 | BAA02g10120 | A02 | 4479521 | G | A | missense_variant | MODERATE | c.200C>T|p.Ala67Val |
S95 |
5 | BAA02g10120 | A02 | 4479582 | G | A | synonymous_variant | LOW | c.139C>T|p.Leu47Leu |
S17 |
6 | BAA02g10120 | A02 | 4480536 | G | A | upstream_gene_variant | MODIFIER | c.-816C>T| |
S236 |