Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00020 | A01 | 2038 | G | A | upstream_gene_variant | MODIFIER | c.-4862G>A| |
S44 |
2 | BAA01g00020 | A01 | 2079 | G | A | upstream_gene_variant | MODIFIER | c.-4821G>A| |
S228 |
3 | BAA01g00020 | A01 | 2666 | G | A | upstream_gene_variant | MODIFIER | c.-4234G>A| |
S173 |
4 | BAA01g00020 | A01 | 3408 | C | T | upstream_gene_variant | MODIFIER | c.-3492C>T| |
S277 S41 |
5 | BAA01g00020 | A01 | 3983 | G | A | upstream_gene_variant | MODIFIER | c.-2917G>A| |
S181 |
6 | BAA01g00020 | A01 | 4262 | G | A | upstream_gene_variant | MODIFIER | c.-2638G>A| |
S136 |
7 | BAA01g00020 | A01 | 4469 | C | T | upstream_gene_variant | MODIFIER | c.-2431C>T| |
S249 |
8 | BAA01g00020 | A01 | 6140 | C | T | upstream_gene_variant | MODIFIER | c.-760C>T| |
S159 S243 |
9 | BAA01g00020 | A01 | 7771 | C | T | missense_variant | MODERATE | c.167C>T|p.Ala56Val |
S137 |
10 | BAA01g00020 | A01 | 7860 | C | T | missense_variant | MODERATE | c.256C>T|p.Arg86Cys |
S233 |