Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27960 | A01 | 17040741 | G | A | upstream_gene_variant | MODIFIER | c.-2661G>A| |
S197 |
2 | BAA01g27960 | A01 | 17040752 | C | T | upstream_gene_variant | MODIFIER | c.-2650C>T| |
S282 |
3 | BAA01g27960 | A01 | 17040757 | A | C | upstream_gene_variant | MODIFIER | c.-2645A>C| |
S11 S116 S135 S281 |
4 | BAA01g27960 | A01 | 17041454 | G | A | upstream_gene_variant | MODIFIER | c.-1948G>A| |
S61 |
5 | BAA01g27960 | A01 | 17042396 | C | T | upstream_gene_variant | MODIFIER | c.-1006C>T| |
S264 |
6 | BAA01g27960 | A01 | 17043339 | C | T | upstream_gene_variant | MODIFIER | c.-63C>T| |
S155 S211 |
7 | BAA01g27960 | A01 | 17043343 | C | T | upstream_gene_variant | MODIFIER | c.-59C>T| |
S184 |
8 | BAA01g27960 | A01 | 17043581 | G | A | synonymous_variant | LOW | c.180G>A|p.Leu60Leu |
S260 |
9 | BAA01g27960 | A01 | 17044094 | G | A | synonymous_variant | LOW | c.693G>A|p.Arg231Arg |
S9 |
10 | BAA01g27960 | A01 | 17044171 | G | A | missense_variant | MODERATE | c.770G>A|p.Cys257Tyr |
S221 |
11 | BAA01g27960 | A01 | 17045368 | G | T | missense_variant | MODERATE | c.1589G>T|p.Cys530Phe |
S76 |