Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45360 | A02 | 37152578 | C | T | missense_variant | MODERATE | c.485G>A|p.Arg162Lys |
S119 |
2 | BAA02g45360 | A02 | 37154625 | G | A | synonymous_variant | LOW | c.63C>T|p.Phe21Phe |
S280 |
3 | BAA02g45360 | A02 | 37155104 | C | T | upstream_gene_variant | MODIFIER | c.-417G>A| |
S107 |
4 | BAA02g45360 | A02 | 37155795 | G | A | upstream_gene_variant | MODIFIER | c.-1108C>T| |
S148 S31 |
5 | BAA02g45360 | A02 | 37156597 | G | A | upstream_gene_variant | MODIFIER | c.-1910C>T| |
S261 |
6 | BAA02g45360 | A02 | 37156639 | G | A | upstream_gene_variant | MODIFIER | c.-1952C>T| |
S279 |
7 | BAA02g45360 | A02 | 37156700 | C | T | upstream_gene_variant | MODIFIER | c.-2013G>A| |
S59 |
8 | BAA02g45360 | A02 | 37158733 | G | A | upstream_gene_variant | MODIFIER | c.-4046C>T| |
S111 |
9 | BAA02g45360 | A02 | 37159157 | C | T | upstream_gene_variant | MODIFIER | c.-4470G>A| |
S112 |