Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04680 | A02 | 2032065 | C | T | missense_variant | MODERATE | c.298G>A|p.Asp100Asn |
S178 |
2 | BAA02g04680 | A02 | 2032493 | C | T | upstream_gene_variant | MODIFIER | c.-60G>A| |
S55 |
3 | BAA02g04680 | A02 | 2032862 | C | T | upstream_gene_variant | MODIFIER | c.-429G>A| |
S301 S304 |
4 | BAA02g04680 | A02 | 2033199 | G | A | upstream_gene_variant | MODIFIER | c.-766C>T| |
S78 |
5 | BAA02g04680 | A02 | 2034352 | G | A | upstream_gene_variant | MODIFIER | c.-1919C>T| |
S228 |
6 | BAA02g04680 | A02 | 2034578 | C | T | upstream_gene_variant | MODIFIER | c.-2145G>A| |
S255 |
7 | BAA02g04680 | A02 | 2034855 | C | T | upstream_gene_variant | MODIFIER | c.-2422G>A| |
S207 |
8 | BAA02g04680 | A02 | 2035251 | C | T | upstream_gene_variant | MODIFIER | c.-2818G>A| |
S8 |
9 | BAA02g04680 | A02 | 2035488 | G | A | upstream_gene_variant | MODIFIER | c.-3055C>T| |
S297 |
10 | BAA02g04680 | A02 | 2036326 | C | T | upstream_gene_variant | MODIFIER | c.-3893G>A| |
S65 |
11 | BAA02g04680 | A02 | 2036395 | C | T | upstream_gene_variant | MODIFIER | c.-3962G>A| |
S195 |