Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00900 | A08 | 685909 | C | T | downstream_gene_variant | MODIFIER | c.*4246G>A| |
S280 |
2 | BAA08g00900 | A08 | 686931 | C | T | downstream_gene_variant | MODIFIER | c.*3224G>A| |
S111 |
3 | BAA08g00900 | A08 | 687334 | C | T | downstream_gene_variant | MODIFIER | c.*2821G>A| |
S36 |
4 | BAA08g00900 | A08 | 687386 | C | T | downstream_gene_variant | MODIFIER | c.*2769G>A| |
S206 S26 |
5 | BAA08g00900 | A08 | 688632 | C | T | downstream_gene_variant | MODIFIER | c.*1523G>A| |
S236 |
6 | BAA08g00900 | A08 | 689637 | G | A | downstream_gene_variant | MODIFIER | c.*518C>T| |
S95 |
7 | BAA08g00900 | A08 | 690260 | C | T | synonymous_variant | LOW | c.453G>A|p.Glu151Glu |
S293 |
8 | BAA08g00900 | A08 | 690951 | G | A | missense_variant | MODERATE | c.154C>T|p.Pro52Ser |
S182 |
9 | BAA08g00900 | A08 | 691541 | C | T | upstream_gene_variant | MODIFIER | c.-362G>A| |
S136 |
10 | BAA08g00900 | A08 | 691850 | C | T | upstream_gene_variant | MODIFIER | c.-671G>A| |
S155 |
11 | BAA08g00900 | A08 | 695644 | C | T | upstream_gene_variant | MODIFIER | c.-4465G>A| |
S47 |
12 | BAA08g00900 | A08 | 695657 | C | T | upstream_gene_variant | MODIFIER | c.-4478G>A| |
S184 |
13 | BAA08g00900 | A08 | 695837 | G | A | upstream_gene_variant | MODIFIER | c.-4658C>T| |
S259 |
14 | BAA08g00900 | A08 | 695990 | G | A | upstream_gene_variant | MODIFIER | c.-4811C>T| |
S308 |