Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19660 | A05 | 11680955 | C | T | downstream_gene_variant | MODIFIER | c.*2207G>A| |
S164 |
2 | BAA05g19660 | A05 | 11681028 | G | A | downstream_gene_variant | MODIFIER | c.*2134C>T| |
S23 |
3 | BAA05g19660 | A05 | 11681588 | C | T | downstream_gene_variant | MODIFIER | c.*1574G>A| |
S191 |
4 | BAA05g19660 | A05 | 11681653 | G | A | downstream_gene_variant | MODIFIER | c.*1509C>T| |
S39 |
5 | BAA05g19660 | A05 | 11681975 | G | A | downstream_gene_variant | MODIFIER | c.*1187C>T| |
S219 S72 |
6 | BAA05g19660 | A05 | 11682323 | G | A | downstream_gene_variant | MODIFIER | c.*839C>T| |
S168 |
7 | BAA05g19660 | A05 | 11682326 | G | A | downstream_gene_variant | MODIFIER | c.*836C>T| |
S80 |
8 | BAA05g19660 | A05 | 11682423 | C | T | downstream_gene_variant | MODIFIER | c.*739G>A| |
S270 |
9 | BAA05g19660 | A05 | 11683459 | C | T | intron_variant | MODIFIER | c.548-20G>A| |
S146 |
10 | BAA05g19660 | A05 | 11683636 | G | A | intron_variant | MODIFIER | c.445-16C>T| |
S109 |
11 | BAA05g19660 | A05 | 11684335 | C | T | missense_variant | MODERATE | c.85G>A|p.Ala29Thr |
S118 |
12 | BAA05g19660 | A05 | 11684499 | G | A | upstream_gene_variant | MODIFIER | c.-80C>T| |
S32 |
13 | BAA05g19660 | A05 | 11684843 | G | A | upstream_gene_variant | MODIFIER | c.-424C>T| |
S279 |
14 | BAA05g19660 | A05 | 11685162 | G | A | upstream_gene_variant | MODIFIER | c.-743C>T| |
S208 S219 |
15 | BAA05g19660 | A05 | 11688312 | C | T | upstream_gene_variant | MODIFIER | c.-3893G>A| |
S42 |