Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16990 | A10 | 16556540 | G | A | upstream_gene_variant | MODIFIER | c.-4296G>A| |
S174 S27 |
2 | BAA10g16990 | A10 | 16556933 | G | A | upstream_gene_variant | MODIFIER | c.-3903G>A| |
S217 |
3 | BAA10g16990 | A10 | 16558616 | C | T | upstream_gene_variant | MODIFIER | c.-2220C>T| |
S299 |
4 | BAA10g16990 | A10 | 16558983 | C | T | upstream_gene_variant | MODIFIER | c.-1853C>T| |
S249 |
5 | BAA10g16990 | A10 | 16560201 | G | A | upstream_gene_variant | MODIFIER | c.-635G>A| |
S155 S211 |
6 | BAA10g16990 | A10 | 16561625 | G | A | missense_variant | MODERATE | c.533G>A|p.Arg178Lys |
S158 |
7 | BAA10g16990 | A10 | 16561840 | C | T | intron_variant | MODIFIER | c.649+99C>T| |
S19 |
8 | BAA10g16990 | A10 | 16562704 | G | A | intron_variant | MODIFIER | c.650-446G>A| |
S178 |
9 | BAA10g16990 | A10 | 16565644 | G | A | downstream_gene_variant | MODIFIER | c.*2009G>A| |
S67 |
10 | BAA10g16990 | A10 | 16566361 | C | T | downstream_gene_variant | MODIFIER | c.*2726C>T| |
S282 |
11 | BAA10g16990 | A10 | 16566694 | G | A | downstream_gene_variant | MODIFIER | c.*3059G>A| |
S132 S215 S89 |
12 | BAA10g16990 | A10 | 16568003 | C | T | downstream_gene_variant | MODIFIER | c.*4368C>T| |
S177 |
13 | BAA10g16990 | A10 | 16568176 | C | T | downstream_gene_variant | MODIFIER | c.*4541C>T| |
S47 |