Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25120 | A02 | 13738053 | G | A | upstream_gene_variant | MODIFIER | c.-3559G>A| |
S217 S248 |
2 | BAA02g25120 | A02 | 13738059 | C | T | upstream_gene_variant | MODIFIER | c.-3553C>T| |
S18 |
3 | BAA02g25120 | A02 | 13738124 | G | A | upstream_gene_variant | MODIFIER | c.-3488G>A| |
S79 S91 |
4 | BAA02g25120 | A02 | 13739034 | C | T | upstream_gene_variant | MODIFIER | c.-2578C>T| |
S162 |
5 | BAA02g25120 | A02 | 13740542 | C | T | upstream_gene_variant | MODIFIER | c.-1070C>T| |
S271 |
6 | BAA02g25120 | A02 | 13740623 | C | T | upstream_gene_variant | MODIFIER | c.-989C>T| |
S42 |
7 | BAA02g25120 | A02 | 13740735 | C | T | upstream_gene_variant | MODIFIER | c.-877C>T| |
S178 |
8 | BAA02g25120 | A02 | 13742622 | G | A | missense_variant | MODERATE | c.493G>A|p.Asp165Asn |
S136 |
9 | BAA02g25120 | A02 | 13742628 | G | A | missense_variant | MODERATE | c.499G>A|p.Glu167Lys |
S111 |
10 | BAA02g25120 | A02 | 13744472 | C | T | synonymous_variant | LOW | c.1533C>T|p.Arg511Arg |
S270 |