Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45460 | A02 | 37214558 | C | T | missense_variant | MODERATE | c.592G>A|p.Glu198Lys |
S238 |
2 | BAA02g45460 | A02 | 37215271 | C | T | missense_variant | MODERATE | c.136G>A|p.Glu46Lys |
S3 |
3 | BAA02g45460 | A02 | 37218310 | G | A | upstream_gene_variant | MODIFIER | c.-2820C>T| |
S73 |
4 | BAA02g45460 | A02 | 37218802 | C | T | upstream_gene_variant | MODIFIER | c.-3312G>A| |
S201 |
5 | BAA02g45460 | A02 | 37218982 | C | T | upstream_gene_variant | MODIFIER | c.-3492G>A| |
S87 |
6 | BAA02g45460 | A02 | 37219148 | G | A | upstream_gene_variant | MODIFIER | c.-3658C>T| |
S297 |
7 | BAA02g45460 | A02 | 37220437 | G | A | upstream_gene_variant | MODIFIER | c.-4947C>T| |
S166 |
8 | BAA02g45460 | A02 | 37220471 | G | A | upstream_gene_variant | MODIFIER | c.-4981C>T| |
S67 |