Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g20790 | A05 | 12957964 | G | A | upstream_gene_variant | MODIFIER | c.-4885G>A| |
S151 S263 |
2 | BAA05g20790 | A05 | 12958151 | C | T | upstream_gene_variant | MODIFIER | c.-4698C>T| |
S180 |
3 | BAA05g20790 | A05 | 12959179 | G | A | upstream_gene_variant | MODIFIER | c.-3670G>A| |
S161 |
4 | BAA05g20790 | A05 | 12959218 | C | T | upstream_gene_variant | MODIFIER | c.-3631C>T| |
S105 S106 |
5 | BAA05g20790 | A05 | 12959407 | C | T | upstream_gene_variant | MODIFIER | c.-3442C>T| |
S17 |
6 | BAA05g20790 | A05 | 12959436 | C | T | upstream_gene_variant | MODIFIER | c.-3413C>T| |
S59 |
7 | BAA05g20790 | A05 | 12959569 | C | T | upstream_gene_variant | MODIFIER | c.-3280C>T| |
S28 |
8 | BAA05g20790 | A05 | 12963168 | G | A | missense_variant | MODERATE | c.320G>A|p.Gly107Glu |
S15 |
9 | BAA05g20790 | A05 | 12967111 | G | A | downstream_gene_variant | MODIFIER | c.*3729G>A| |
S264 |
10 | BAA05g20790 | A05 | 12968164 | G | A | downstream_gene_variant | MODIFIER | c.*4782G>A| |
S6 |