| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 182051 | BAA02g21220 | A02 | 11365534 | G | A | upstream_gene_variant | MODIFIER | c.-4305C>T| |
S7 |
| 182052 | BAA02g21220 | A02 | 11365539 | C | T | upstream_gene_variant | MODIFIER | c.-4310G>A| |
S49 |
| 182053 | BAA02g21220 | A02 | 11365557 | G | A | upstream_gene_variant | MODIFIER | c.-4328C>T| |
S191 |
| 182054 | BAA02g21220 | A02 | 11365886 | G | A | upstream_gene_variant | MODIFIER | c.-4657C>T| |
S44 |
| 182055 | BAA02g21220 | A02 | 11366076 | G | A | upstream_gene_variant | MODIFIER | c.-4847C>T| |
S148 |
| 182056 | BAA02g21220-BAA02g21230 | A02 | 11366918 | C | T | intergenic_region | MODIFIER | n.11366918C>T| |
S81 |
| 182057 | BAA02g21220-BAA02g21230 | A02 | 11367022 | G | A | intergenic_region | MODIFIER | n.11367022G>A| |
S110 |
| 182058 | BAA02g21230 | A02 | 11368548 | C | T | upstream_gene_variant | MODIFIER | c.-3703C>T| |
S112 |
| 182059 | BAA02g21230 | A02 | 11369874 | G | A | upstream_gene_variant | MODIFIER | c.-2377G>A| |
S33 |
| 182060 | BAA02g21230 | A02 | 11369876 | G | A | upstream_gene_variant | MODIFIER | c.-2375G>A| |
S17 |
| 182061 | BAA02g21230 | A02 | 11369904 | C | T | upstream_gene_variant | MODIFIER | c.-2347C>T| |
S77 S82 |
| 182062 | BAA02g21230 | A02 | 11370362 | G | A | upstream_gene_variant | MODIFIER | c.-1889G>A| |
S19 |
| 182063 | BAA02g21230 | A02 | 11370973 | C | T | upstream_gene_variant | MODIFIER | c.-1278C>T| |
S71 |
| 182064 | BAA02g21230 | A02 | 11373568 | G | A | downstream_gene_variant | MODIFIER | c.*1057G>A| |
S256 |
| 182065 | BAA02g21230 | A02 | 11373835 | C | T | downstream_gene_variant | MODIFIER | c.*1324C>T| |
S183 S198 |
| 182066 | BAA02g21230 | A02 | 11373841 | G | A | downstream_gene_variant | MODIFIER | c.*1330G>A| |
S279 |
| 182067 | BAA02g21240 | A02 | 11376880 | C | T | missense_variant | MODERATE | c.449G>A|p.Arg150Lys |
S221 |
| 182068 | BAA02g21240 | A02 | 11377151 | G | A | missense_variant | MODERATE | c.178C>T|p.Pro60Ser |
S133 |
| 182069 | BAA02g21240 | A02 | 11377378 | G | A | upstream_gene_variant | MODIFIER | c.-50C>T| |
S148 |
| 182070 | BAA02g21240 | A02 | 11377853 | G | A | upstream_gene_variant | MODIFIER | c.-525C>T| |
S59 |
| 182071 | BAA02g21240 | A02 | 11378002 | G | A | upstream_gene_variant | MODIFIER | c.-674C>T| |
S256 |
| 182072 | BAA02g21240 | A02 | 11378666 | C | T | upstream_gene_variant | MODIFIER | c.-1338G>A| |
S262 |
| 182073 | BAA02g21240 | A02 | 11378945 | C | T | upstream_gene_variant | MODIFIER | c.-1617G>A| |
S130 |
| 182074 | BAA02g21240 | A02 | 11379608 | C | T | upstream_gene_variant | MODIFIER | c.-2280G>A| |
S53 |
| 182075 | BAA02g21240 | A02 | 11380683 | G | A | upstream_gene_variant | MODIFIER | c.-3355C>T| |
S206 S26 |