Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42770 | A02 | 35599146 | G | A | synonymous_variant | LOW | c.2178C>T|p.Tyr726Tyr |
S200 |
2 | BAA02g42770 | A02 | 35599384 | C | T | missense_variant | MODERATE | c.1940G>A|p.Arg647Lys |
S201 |
3 | BAA02g42770 | A02 | 35600006 | C | T | missense_variant | MODERATE | c.1478G>A|p.Arg493His |
S189 |
4 | BAA02g42770 | A02 | 35600039 | G | A | missense_variant | MODERATE | c.1445C>T|p.Thr482Met |
S81 S85 |
5 | BAA02g42770 | A02 | 35600513 | C | T | missense_variant | MODERATE | c.1153G>A|p.Glu385Lys |
S3 |
6 | BAA02g42770 | A02 | 35603454 | C | T | upstream_gene_variant | MODIFIER | c.-1016G>A| |
S123 |
7 | BAA02g42770 | A02 | 35605564 | G | A | upstream_gene_variant | MODIFIER | c.-3126C>T| |
S136 |
8 | BAA02g42770 | A02 | 35605625 | C | T | upstream_gene_variant | MODIFIER | c.-3187G>A| |
S129 |
9 | BAA02g42770 | A02 | 35606999 | A | C | upstream_gene_variant | MODIFIER | c.-4561T>G| |
S107 |