Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26470 | A05 | 31100734 | C | T | upstream_gene_variant | MODIFIER | c.-4056C>T| |
S140 S279 |
2 | BAA05g26470 | A05 | 31101348 | G | A | upstream_gene_variant | MODIFIER | c.-3442G>A| |
S156 |
3 | BAA05g26470 | A05 | 31101458 | G | A | upstream_gene_variant | MODIFIER | c.-3332G>A| |
S138 |
4 | BAA05g26470 | A05 | 31101966 | C | T | upstream_gene_variant | MODIFIER | c.-2824C>T| |
S2 |
5 | BAA05g26470 | A05 | 31103766 | C | T | upstream_gene_variant | MODIFIER | c.-1024C>T| |
S63 |
6 | BAA05g26470 | A05 | 31104396 | C | T | upstream_gene_variant | MODIFIER | c.-394C>T| |
S12 |
7 | BAA05g26470 | A05 | 31104438 | G | A | upstream_gene_variant | MODIFIER | c.-352G>A| |
S252 |
8 | BAA05g26470 | A05 | 31105676 | C | T | missense_variant | MODERATE | c.251C>T|p.Ala84Val |
S153 |
9 | BAA05g26470 | A05 | 31106492 | C | T | missense_variant | MODERATE | c.497C>T|p.Pro166Leu |
S73 |
10 | BAA05g26470 | A05 | 31107074 | C | T | missense_variant | MODERATE | c.646C>T|p.Leu216Phe |
S12 |
11 | BAA05g26470 | A05 | 31109956 | C | T | downstream_gene_variant | MODIFIER | c.*2506C>T| |
S272 |