Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44380 | A02 | 36569007 | G | A | missense_variant | MODERATE | c.510G>A|p.Met170Ile |
S35 |
2 | BAA02g44380 | A02 | 36569459 | G | A | missense_variant | MODERATE | c.635G>A|p.Arg212Lys |
S54 |
3 | BAA02g44380 | A02 | 36569628 | C | T | synonymous_variant | LOW | c.804C>T|p.Phe268Phe |
S218 |
4 | BAA02g44380 | A02 | 36569860 | C | T | synonymous_variant | LOW | c.948C>T|p.Tyr316Tyr |
S171 |
5 | BAA02g44380 | A02 | 36574139 | G | A | downstream_gene_variant | MODIFIER | c.*4237G>A| |
S272 |