Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20760 | A02 | 11029096 | G | A | upstream_gene_variant | MODIFIER | c.-4190G>A| |
S72 |
2 | BAA02g20760 | A02 | 11029347 | C | T | upstream_gene_variant | MODIFIER | c.-3939C>T| |
S302 |
3 | BAA02g20760 | A02 | 11030503 | C | T | upstream_gene_variant | MODIFIER | c.-2783C>T| |
S157 S166 |
4 | BAA02g20760 | A02 | 11030576 | G | A | upstream_gene_variant | MODIFIER | c.-2710G>A| |
S206 S26 |
5 | BAA02g20760 | A02 | 11030854 | G | A | upstream_gene_variant | MODIFIER | c.-2432G>A| |
S155 S211 |
6 | BAA02g20760 | A02 | 11031432 | C | T | upstream_gene_variant | MODIFIER | c.-1854C>T| |
S71 |
7 | BAA02g20760 | A02 | 11033650 | C | T | missense_variant | MODERATE | c.290C>T|p.Thr97Ile |
S144 |
8 | BAA02g20760 | A02 | 11034127 | G | A | missense_variant | MODERATE | c.767G>A|p.Arg256Lys |
S157 |
9 | BAA02g20760 | A02 | 11035102 | C | T | intron_variant | MODIFIER | c.1367-85C>T| |
S179 |
10 | BAA02g20760 | A02 | 11035139 | G | A | intron_variant | MODIFIER | c.1367-48G>A| |
S241 |
11 | BAA02g20760 | A02 | 11036141 | G | A | downstream_gene_variant | MODIFIER | c.*370G>A| |
S303 |
12 | BAA02g20760 | A02 | 11036304 | G | A | downstream_gene_variant | MODIFIER | c.*533G>A| |
S259 |