Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09340 | A05 | 4716082 | G | T | upstream_gene_variant | MODIFIER | c.-3909G>T| |
S116 |
2 | BAA05g09340 | A05 | 4717022 | G | A | upstream_gene_variant | MODIFIER | c.-2969G>A| |
S2 |
3 | BAA05g09340 | A05 | 4717324 | C | T | upstream_gene_variant | MODIFIER | c.-2667C>T| |
S98 |
4 | BAA05g09340 | A05 | 4717559 | G | A | upstream_gene_variant | MODIFIER | c.-2432G>A| |
S210 S225 |
5 | BAA05g09340 | A05 | 4718634 | C | T | upstream_gene_variant | MODIFIER | c.-1357C>T| |
S209 |
6 | BAA05g09340 | A05 | 4719559 | C | T | upstream_gene_variant | MODIFIER | c.-432C>T| |
S12 |
7 | BAA05g09340 | A05 | 4719878 | C | T | upstream_gene_variant | MODIFIER | c.-113C>T| |
S60 |
8 | BAA05g09340 | A05 | 4721002 | G | A | missense_variant | MODERATE | c.524G>A|p.Gly175Glu |
S262 |
9 | BAA05g09340 | A05 | 4721616 | G | A | missense_variant | MODERATE | c.895G>A|p.Asp299Asn |
S219 |
10 | BAA05g09340 | A05 | 4722324 | G | A | downstream_gene_variant | MODIFIER | c.*499G>A| |
S294 |
11 | BAA05g09340 | A05 | 4724180 | C | T | downstream_gene_variant | MODIFIER | c.*2355C>T| |
S163 |
12 | BAA05g09340 | A05 | 4724335 | C | T | downstream_gene_variant | MODIFIER | c.*2510C>T| |
S284 |
13 | BAA05g09340 | A05 | 4725046 | G | A | downstream_gene_variant | MODIFIER | c.*3221G>A| |
S238 |