Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19450 | A02 | 10092242 | C | T | upstream_gene_variant | MODIFIER | c.-4146C>T| |
S94 |
2 | BAA02g19450 | A02 | 10092604 | C | T | upstream_gene_variant | MODIFIER | c.-3784C>T| |
S44 |
3 | BAA02g19450 | A02 | 10092696 | G | A | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S295 |
4 | BAA02g19450 | A02 | 10092879 | C | T | upstream_gene_variant | MODIFIER | c.-3509C>T| |
S302 |
5 | BAA02g19450 | A02 | 10092888 | C | T | upstream_gene_variant | MODIFIER | c.-3500C>T| |
S262 |
6 | BAA02g19450 | A02 | 10093003 | C | T | upstream_gene_variant | MODIFIER | c.-3385C>T| |
S267 |
7 | BAA02g19450 | A02 | 10093028 | C | T | upstream_gene_variant | MODIFIER | c.-3360C>T| |
S32 |
8 | BAA02g19450 | A02 | 10093273 | G | A | upstream_gene_variant | MODIFIER | c.-3115G>A| |
S28 |
9 | BAA02g19450 | A02 | 10093366 | G | A | upstream_gene_variant | MODIFIER | c.-3022G>A| |
S231 |
10 | BAA02g19450 | A02 | 10093799 | C | T | upstream_gene_variant | MODIFIER | c.-2589C>T| |
S299 |
11 | BAA02g19450 | A02 | 10093805 | G | A | upstream_gene_variant | MODIFIER | c.-2583G>A| |
S269 |
12 | BAA02g19450 | A02 | 10095692 | C | T | upstream_gene_variant | MODIFIER | c.-696C>T| |
S97 |
13 | BAA02g19450 | A02 | 10098425 | G | A | splice_region_variant&synonymous_variant | LOW | c.738G>A|p.Ala246Ala |
S169 |
14 | BAA02g19450 | A02 | 10102673 | C | T | downstream_gene_variant | MODIFIER | c.*3627C>T| |
S175 |
15 | BAA02g19450 | A02 | 10102707 | G | A | downstream_gene_variant | MODIFIER | c.*3661G>A| |
S289 S290 |
16 | BAA02g19450 | A02 | 10102939 | G | A | downstream_gene_variant | MODIFIER | c.*3893G>A| |
S126 |
17 | BAA02g19450 | A02 | 10103725 | G | A | downstream_gene_variant | MODIFIER | c.*4679G>A| |
S34 |
18 | BAA02g19450 | A02 | 10103727 | G | A | downstream_gene_variant | MODIFIER | c.*4681G>A| |
S213 |