Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27660 | A02 | 15568002 | G | A | upstream_gene_variant | MODIFIER | c.-873G>A| |
S19 |
2 | BAA02g27660 | A02 | 15568849 | C | T | upstream_gene_variant | MODIFIER | c.-26C>T| |
S115 |
3 | BAA02g27660 | A02 | 15568966 | G | A | missense_variant | MODERATE | c.92G>A|p.Gly31Asp |
S293 |
4 | BAA02g27660 | A02 | 15569061 | G | A | missense_variant | MODERATE | c.187G>A|p.Asp63Asn |
S202 |
5 | BAA02g27660 | A02 | 15569393 | G | A | synonymous_variant | LOW | c.519G>A|p.Gln173Gln |
S202 |
6 | BAA02g27660 | A02 | 15569473 | C | T | missense_variant | MODERATE | c.599C>T|p.Pro200Leu |
S268 |
7 | BAA02g27660 | A02 | 15569530 | G | A | missense_variant | MODERATE | c.656G>A|p.Ser219Asn |
S251 |
8 | BAA02g27660 | A02 | 15573372 | C | T | downstream_gene_variant | MODIFIER | c.*3814C>T| |
S167 |
9 | BAA02g27660 | A02 | 15574326 | G | A | downstream_gene_variant | MODIFIER | c.*4768G>A| |
S37 |