Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11380 | A02 | 5142090 | G | A | synonymous_variant | LOW | c.1227C>T|p.His409His |
S303 |
2 | BAA02g11380 | A02 | 5142438 | C | T | synonymous_variant | LOW | c.879G>A|p.Arg293Arg |
S278 |
3 | BAA02g11380 | A02 | 5142593 | G | A | intron_variant | MODIFIER | c.772-48C>T| |
S287 |
4 | BAA02g11380 | A02 | 5142831 | C | T | intron_variant | MODIFIER | c.772-286G>A| |
S200 |
5 | BAA02g11380 | A02 | 5143277 | C | T | missense_variant | MODERATE | c.625G>A|p.Asp209Asn |
S171 |
6 | BAA02g11380 | A02 | 5146143 | G | A | upstream_gene_variant | MODIFIER | c.-1797C>T| |
S122 |
7 | BAA02g11380 | A02 | 5147953 | G | A | upstream_gene_variant | MODIFIER | c.-3607C>T| |
S247 |
8 | BAA02g11380 | A02 | 5148766 | C | T | upstream_gene_variant | MODIFIER | c.-4420G>A| |
S267 |