Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20590 | A01 | 10161256 | C | T | upstream_gene_variant | MODIFIER | c.-274C>T| |
S179 |
2 | BAA01g20590 | A01 | 10161666 | G | A | missense_variant | MODERATE | c.137G>A|p.Arg46His |
S108 S79 S91 |
3 | BAA01g20590 | A01 | 10164198 | G | A | intron_variant | MODIFIER | c.1171-64G>A| |
S59 |
4 | BAA01g20590 | A01 | 10164665 | C | T | downstream_gene_variant | MODIFIER | c.*146C>T| |
S38 |
5 | BAA01g20590 | A01 | 10165517 | G | A | downstream_gene_variant | MODIFIER | c.*998G>A| |
S117 |
6 | BAA01g20590 | A01 | 10167277 | C | T | downstream_gene_variant | MODIFIER | c.*2758C>T| |
S135 |
7 | BAA01g20590 | A01 | 10168750 | C | T | downstream_gene_variant | MODIFIER | c.*4231C>T| |
S81 |
8 | BAA01g20590 | A01 | 10169008 | C | T | downstream_gene_variant | MODIFIER | c.*4489C>T| |
S18 |
9 | BAA01g20590 | A01 | 10169399 | G | A | downstream_gene_variant | MODIFIER | c.*4880G>A| |
S6 |