Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09690 | A05 | 4919422 | G | A | upstream_gene_variant | MODIFIER | c.-4794G>A| |
S294 |
2 | BAA05g09690 | A05 | 4919515 | G | A | upstream_gene_variant | MODIFIER | c.-4701G>A| |
S173 |
3 | BAA05g09690 | A05 | 4919702 | G | A | upstream_gene_variant | MODIFIER | c.-4514G>A| |
S11 |
4 | BAA05g09690 | A05 | 4920964 | C | T | upstream_gene_variant | MODIFIER | c.-3252C>T| |
S171 |
5 | BAA05g09690 | A05 | 4921065 | G | A | upstream_gene_variant | MODIFIER | c.-3151G>A| |
S115 |
6 | BAA05g09690 | A05 | 4921466 | G | A | upstream_gene_variant | MODIFIER | c.-2750G>A| |
S32 |
7 | BAA05g09690 | A05 | 4922762 | G | A | upstream_gene_variant | MODIFIER | c.-1454G>A| |
S150 |
8 | BAA05g09690 | A05 | 4923794 | C | T | upstream_gene_variant | MODIFIER | c.-422C>T| |
S117 |
9 | BAA05g09690 | A05 | 4923966 | G | A | upstream_gene_variant | MODIFIER | c.-250G>A| |
S252 |
10 | BAA05g09690 | A05 | 4924359 | G | A | intron_variant | MODIFIER | c.107+37G>A| |
S279 |
11 | BAA05g09690 | A05 | 4924554 | G | A | missense_variant | MODERATE | c.160G>A|p.Asp54Asn |
S80 |