Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42000 | A02 | 35047503 | G | A | upstream_gene_variant | MODIFIER | c.-4097G>A| |
S62 |
2 | BAA02g42000 | A02 | 35051844 | G | A | missense_variant | MODERATE | c.245G>A|p.Ser82Asn |
S176 |
3 | BAA02g42000 | A02 | 35052433 | C | T | synonymous_variant | LOW | c.480C>T|p.Ile160Ile |
S242 |
4 | BAA02g42000 | A02 | 35053407 | G | A | missense_variant | MODERATE | c.1162G>A|p.Ala388Thr |
S35 |
5 | BAA02g42000 | A02 | 35054144 | C | T | synonymous_variant | LOW | c.1818C>T|p.Pro606Pro |
S116 |
6 | BAA02g42000 | A02 | 35054304 | C | T | synonymous_variant | LOW | c.1899C>T|p.Ile633Ile |
S239 |
7 | BAA02g42000 | A02 | 35054461 | C | T | missense_variant | MODERATE | c.1979C>T|p.Ser660Phe |
S194 |
8 | BAA02g42000 | A02 | 35055219 | G | A | synonymous_variant | LOW | c.2532G>A|p.Ser844Ser |
S191 S92 |
9 | BAA02g42000 | A02 | 35057053 | C | A | downstream_gene_variant | MODIFIER | c.*478C>A| |
S167 |