Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42490 | A02 | 35389085 | G | A | upstream_gene_variant | MODIFIER | c.-41G>A| |
S264 |
2 | BAA02g42490 | A02 | 35389504 | G | A | missense_variant | MODERATE | c.379G>A|p.Asp127Asn |
S207 |
3 | BAA02g42490 | A02 | 35389947 | G | A | synonymous_variant | LOW | c.822G>A|p.Glu274Glu |
S286 |
4 | BAA02g42490 | A02 | 35390846 | G | A | synonymous_variant | LOW | c.1134G>A|p.Val378Val |
S292 |
5 | BAA02g42490 | A02 | 35390906 | G | A | synonymous_variant | LOW | c.1194G>A|p.Ser398Ser |
S37 |
6 | BAA02g42490 | A02 | 35391180 | G | A | missense_variant&splice_region_variant | MODERATE | c.1468G>A|p.Glu490Lys |
S213 |
7 | BAA02g42490 | A02 | 35393553 | G | A | downstream_gene_variant | MODIFIER | c.*1712G>A| |
S293 |
8 | BAA02g42490 | A02 | 35394058 | C | T | downstream_gene_variant | MODIFIER | c.*2217C>T| |
S43 |