Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g33620 | A02 | 28756066 | C | T | upstream_gene_variant | MODIFIER | c.-639C>T| |
S181 |
2 | BAA02g33620 | A02 | 28756151 | C | T | upstream_gene_variant | MODIFIER | c.-554C>T| |
S140 |
3 | BAA02g33620 | A02 | 28756171 | C | T | upstream_gene_variant | MODIFIER | c.-534C>T| |
S84 S93 |
4 | BAA02g33620 | A02 | 28756325 | G | A | upstream_gene_variant | MODIFIER | c.-380G>A| |
S134 |
5 | BAA02g33620 | A02 | 28756604 | G | A | upstream_gene_variant | MODIFIER | c.-101G>A| |
S207 |
6 | BAA02g33620 | A02 | 28756654 | G | A | upstream_gene_variant | MODIFIER | c.-51G>A| |
S20 |
7 | BAA02g33620 | A02 | 28756738 | G | A | missense_variant | MODERATE | c.34G>A|p.Glu12Lys |
S268 |
8 | BAA02g33620 | A02 | 28757242 | C | T | missense_variant | MODERATE | c.538C>T|p.Pro180Ser |
S203 |
9 | BAA02g33620 | A02 | 28757887 | C | T | missense_variant | MODERATE | c.1106C>T|p.Ala369Val |
S91 |
10 | BAA02g33620 | A02 | 28757979 | G | A | missense_variant | MODERATE | c.1198G>A|p.Ala400Thr |
S86 |
11 | BAA02g33620 | A02 | 28758149 | G | A | synonymous_variant | LOW | c.1368G>A|p.Lys456Lys |
S148 S30 S31 |
12 | BAA02g33620 | A02 | 28758252 | C | A | missense_variant | MODERATE | c.1471C>A|p.Pro491Thr |
S54 |
13 | BAA02g33620 | A02 | 28758830 | G | A | missense_variant | MODERATE | c.1849G>A|p.Glu617Lys |
S168 |
14 | BAA02g33620 | A02 | 28758938 | G | A | downstream_gene_variant | MODIFIER | c.*61G>A| |
S26 |
15 | BAA02g33620 | A02 | 28759222 | C | T | downstream_gene_variant | MODIFIER | c.*345C>T| |
S25 S264 |
16 | BAA02g33620 | A02 | 28759876 | A | C | downstream_gene_variant | MODIFIER | c.*999A>C| |
S197 |
17 | BAA02g33620 | A02 | 28760613 | C | T | downstream_gene_variant | MODIFIER | c.*1736C>T| |
S178 |
18 | BAA02g33620 | A02 | 28761453 | G | A | downstream_gene_variant | MODIFIER | c.*2576G>A| |
S5 |
19 | BAA02g33620 | A02 | 28761717 | G | A | downstream_gene_variant | MODIFIER | c.*2840G>A| |
S188 |
20 | BAA02g33620 | A02 | 28763500 | C | T | downstream_gene_variant | MODIFIER | c.*4623C>T| |
S120 |
21 | BAA02g33620 | A02 | 28763810 | C | T | downstream_gene_variant | MODIFIER | c.*4933C>T| |
S218 |