Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45530 | A02 | 37244072 | C | T | upstream_gene_variant | MODIFIER | c.-408C>T| |
S178 |
2 | BAA02g45530 | A02 | 37244089 | C | T | upstream_gene_variant | MODIFIER | c.-391C>T| |
S123 |
3 | BAA02g45530 | A02 | 37244717 | G | A | missense_variant | MODERATE | c.238G>A|p.Glu80Lys |
S293 |
4 | BAA02g45530 | A02 | 37244941 | C | T | synonymous_variant | LOW | c.462C>T|p.Leu154Leu |
S275 |
5 | BAA02g45530 | A02 | 37245422 | C | T | missense_variant | MODERATE | c.943C>T|p.Pro315Ser |
S120 |
6 | BAA02g45530 | A02 | 37245626 | C | T | missense_variant | MODERATE | c.1147C>T|p.Leu383Phe |
S3 |
7 | BAA02g45530 | A02 | 37246238 | C | T | missense_variant | MODERATE | c.1607C>T|p.Thr536Met |
S273 |
8 | BAA02g45530 | A02 | 37246555 | C | T | missense_variant | MODERATE | c.1754C>T|p.Thr585Ile |
S244 |
9 | BAA02g45530 | A02 | 37246961 | G | A | missense_variant | MODERATE | c.1948G>A|p.Asp650Asn |
S229 |
10 | BAA02g45530 | A02 | 37249046 | C | T | downstream_gene_variant | MODIFIER | c.*39C>T| |
S64 |
11 | BAA02g45530 | A02 | 37249906 | C | T | downstream_gene_variant | MODIFIER | c.*899C>T| |
S133 |