Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41000 | A05 | 39398339 | G | A | missense_variant | MODERATE | c.1336C>T|p.Leu446Phe |
S218 |
2 | BAA05g41000 | A05 | 39399583 | C | T | missense_variant | MODERATE | c.236G>A|p.Gly79Glu |
S221 |
3 | BAA05g41000 | A05 | 39399709 | C | T | missense_variant | MODERATE | c.110G>A|p.Ser37Asn |
S217 S248 |
4 | BAA05g41000 | A05 | 39403204 | C | T | upstream_gene_variant | MODIFIER | c.-3386G>A| |
S203 |