Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20340 | A02 | 10772471 | G | A | upstream_gene_variant | MODIFIER | c.-4330G>A| |
S193 |
2 | BAA02g20340 | A02 | 10773367 | G | A | upstream_gene_variant | MODIFIER | c.-3434G>A| |
S56 |
3 | BAA02g20340 | A02 | 10774315 | G | A | upstream_gene_variant | MODIFIER | c.-2486G>A| |
S188 |
4 | BAA02g20340 | A02 | 10774420 | G | A | upstream_gene_variant | MODIFIER | c.-2381G>A| |
S30 S31 |
5 | BAA02g20340 | A02 | 10774432 | G | A | upstream_gene_variant | MODIFIER | c.-2369G>A| |
S61 |
6 | BAA02g20340 | A02 | 10774951 | G | A | upstream_gene_variant | MODIFIER | c.-1850G>A| |
S59 |
7 | BAA02g20340 | A02 | 10775935 | C | T | upstream_gene_variant | MODIFIER | c.-866C>T| |
S241 |
8 | BAA02g20340 | A02 | 10777219 | C | T | missense_variant | MODERATE | c.419C>T|p.Ser140Leu |
S165 |
9 | BAA02g20340 | A02 | 10777611 | G | A | missense_variant | MODERATE | c.811G>A|p.Gly271Ser |
S192 |
10 | BAA02g20340 | A02 | 10777617 | C | T | missense_variant | MODERATE | c.817C>T|p.Arg273Trp |
S189 |
11 | BAA02g20340 | A02 | 10778112 | G | A | downstream_gene_variant | MODIFIER | c.*343G>A| |
S43 |
12 | BAA02g20340 | A02 | 10778412 | G | A | downstream_gene_variant | MODIFIER | c.*643G>A| |
S294 |
13 | BAA02g20340 | A02 | 10779331 | G | A | downstream_gene_variant | MODIFIER | c.*1562G>A| |
S116 |
14 | BAA02g20340 | A02 | 10779425 | G | A | downstream_gene_variant | MODIFIER | c.*1656G>A| |
S48 |
15 | BAA02g20340 | A02 | 10780241 | C | T | downstream_gene_variant | MODIFIER | c.*2472C>T| |
S249 |
16 | BAA02g20340 | A02 | 10781477 | G | A | downstream_gene_variant | MODIFIER | c.*3708G>A| |
S17 |
17 | BAA02g20340 | A02 | 10781797 | G | A | downstream_gene_variant | MODIFIER | c.*4028G>A| |
S288 |
18 | BAA02g20340 | A02 | 10782289 | C | T | downstream_gene_variant | MODIFIER | c.*4520C>T| |
S124 |