Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01190 | A02 | 555576 | C | T | missense_variant | MODERATE | c.1651G>A|p.Ala551Thr |
S142 |
2 | BAA02g01190 | A02 | 556404 | C | T | missense_variant | MODERATE | c.1111G>A|p.Gly371Arg |
S278 |
3 | BAA02g01190 | A02 | 558053 | C | T | missense_variant | MODERATE | c.248G>A|p.Ser83Asn |
S274 |
4 | BAA02g01190 | A02 | 558355 | C | T | missense_variant | MODERATE | c.34G>A|p.Val12Ile |
S167 |
5 | BAA02g01190 | A02 | 560321 | G | A | upstream_gene_variant | MODIFIER | c.-1933C>T| |
S168 |
6 | BAA02g01190 | A02 | 560390 | G | A | upstream_gene_variant | MODIFIER | c.-2002C>T| |
S136 |
7 | BAA02g01190 | A02 | 560777 | G | A | upstream_gene_variant | MODIFIER | c.-2389C>T| |
S51 |
8 | BAA02g01190 | A02 | 560896 | G | C | upstream_gene_variant | MODIFIER | c.-2508C>G| |
S170 |
9 | BAA02g01190 | A02 | 562312 | G | A | upstream_gene_variant | MODIFIER | c.-3924C>T| |
S208 S93 |
10 | BAA02g01190 | A02 | 562535 | C | T | upstream_gene_variant | MODIFIER | c.-4147G>A| |
S8 |
11 | BAA02g01190 | A02 | 563321 | C | T | upstream_gene_variant | MODIFIER | c.-4933G>A| |
S179 |
12 | BAA02g01190 | A02 | 563335 | C | T | upstream_gene_variant | MODIFIER | c.-4947G>A| |
S144 |