Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45450 | A09 | 50652774 | C | T | upstream_gene_variant | MODIFIER | c.-4914C>T| |
S163 |
2 | BAA09g45450 | A09 | 50654686 | A | T | upstream_gene_variant | MODIFIER | c.-3002A>T| |
S159 S243 S299 |
3 | BAA09g45450 | A09 | 50655179 | C | T | upstream_gene_variant | MODIFIER | c.-2509C>T| |
S65 |
4 | BAA09g45450 | A09 | 50655249 | C | T | upstream_gene_variant | MODIFIER | c.-2439C>T| |
S113 S23 |
5 | BAA09g45450 | A09 | 50655266 | G | A | upstream_gene_variant | MODIFIER | c.-2422G>A| |
S71 |
6 | BAA09g45450 | A09 | 50655566 | C | G | upstream_gene_variant | MODIFIER | c.-2122C>G| |
S269 |
7 | BAA09g45450 | A09 | 50656485 | G | A | upstream_gene_variant | MODIFIER | c.-1203G>A| |
S287 |
8 | BAA09g45450 | A09 | 50657084 | G | A | upstream_gene_variant | MODIFIER | c.-604G>A| |
S107 |
9 | BAA09g45450 | A09 | 50657294 | C | T | upstream_gene_variant | MODIFIER | c.-394C>T| |
S137 S279 |
10 | BAA09g45450 | A09 | 50657854 | C | T | missense_variant | MODERATE | c.167C>T|p.Ser56Phe |
S87 |
11 | BAA09g45450 | A09 | 50657927 | G | A | synonymous_variant | LOW | c.240G>A|p.Gln80Gln |
S176 |
12 | BAA09g45450 | A09 | 50657954 | G | A | synonymous_variant | LOW | c.267G>A|p.Thr89Thr |
S264 |
13 | BAA09g45450 | A09 | 50658092 | G | A | synonymous_variant | LOW | c.405G>A|p.Thr135Thr |
S289 S290 |
14 | BAA09g45450 | A09 | 50658103 | G | A | missense_variant | MODERATE | c.416G>A|p.Gly139Asp |
S46 |
15 | BAA09g45450 | A09 | 50658137 | C | T | synonymous_variant | LOW | c.450C>T|p.Thr150Thr |
S279 |
16 | BAA09g45450 | A09 | 50660172 | G | A | downstream_gene_variant | MODIFIER | c.*1954G>A| |
S46 |
17 | BAA09g45450 | A09 | 50660359 | C | T | downstream_gene_variant | MODIFIER | c.*2141C>T| |
S13 |
18 | BAA09g45450 | A09 | 50660460 | G | A | downstream_gene_variant | MODIFIER | c.*2242G>A| |
S167 |
19 | BAA09g45450 | A09 | 50662231 | C | T | downstream_gene_variant | MODIFIER | c.*4013C>T| |
S138 |
20 | BAA09g45450 | A09 | 50662677 | G | A | downstream_gene_variant | MODIFIER | c.*4459G>A| |
S38 |
21 | BAA09g45450 | A09 | 50662827 | C | T | downstream_gene_variant | MODIFIER | c.*4609C>T| |
S61 |
22 | BAA09g45450 | A09 | 50663016 | C | T | downstream_gene_variant | MODIFIER | c.*4798C>T| |
S295 |