Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10690 | A05 | 5429201 | A | G | upstream_gene_variant | MODIFIER | c.-4522A>G| |
S299 |
2 | BAA05g10690 | A05 | 5429492 | C | T | upstream_gene_variant | MODIFIER | c.-4231C>T| |
S270 |
3 | BAA05g10690 | A05 | 5430900 | C | T | upstream_gene_variant | MODIFIER | c.-2823C>T| |
S247 |
4 | BAA05g10690 | A05 | 5431125 | C | T | upstream_gene_variant | MODIFIER | c.-2598C>T| |
S10 |
5 | BAA05g10690 | A05 | 5431199 | G | A | upstream_gene_variant | MODIFIER | c.-2524G>A| |
S296 |
6 | BAA05g10690 | A05 | 5431413 | C | T | upstream_gene_variant | MODIFIER | c.-2310C>T| |
S13 |
7 | BAA05g10690 | A05 | 5431541 | G | A | upstream_gene_variant | MODIFIER | c.-2182G>A| |
S46 |
8 | BAA05g10690 | A05 | 5432108 | G | A | upstream_gene_variant | MODIFIER | c.-1615G>A| |
S244 |
9 | BAA05g10690 | A05 | 5432742 | C | T | upstream_gene_variant | MODIFIER | c.-981C>T| |
S35 |
10 | BAA05g10690 | A05 | 5432744 | G | A | upstream_gene_variant | MODIFIER | c.-979G>A| |
S109 |
11 | BAA05g10690 | A05 | 5433927 | C | T | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S70 |
12 | BAA05g10690 | A05 | 5438794 | C | T | downstream_gene_variant | MODIFIER | c.*3650C>T| |
S162 |
13 | BAA05g10690 | A05 | 5438911 | C | T | downstream_gene_variant | MODIFIER | c.*3767C>T| |
S51 |
14 | BAA05g10690 | A05 | 5439337 | C | T | downstream_gene_variant | MODIFIER | c.*4193C>T| |
S36 |
15 | BAA05g10690 | A05 | 5439691 | G | A | downstream_gene_variant | MODIFIER | c.*4547G>A| |
S298 |
16 | BAA05g10690 | A05 | 5440066 | C | T | downstream_gene_variant | MODIFIER | c.*4922C>T| |
S12 |