Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g24790 | A01 | 13244973 | C | T | upstream_gene_variant | MODIFIER | c.-2892C>T| |
S270 |
2 | BAA01g24790 | A01 | 13245792 | G | A | upstream_gene_variant | MODIFIER | c.-2073G>A| |
S193 |
3 | BAA01g24790 | A01 | 13246299 | G | A | upstream_gene_variant | MODIFIER | c.-1566G>A| |
S161 |
4 | BAA01g24790 | A01 | 13246371 | G | A | upstream_gene_variant | MODIFIER | c.-1494G>A| |
S199 |
5 | BAA01g24790 | A01 | 13246759 | C | T | upstream_gene_variant | MODIFIER | c.-1106C>T| |
S255 |
6 | BAA01g24790 | A01 | 13246892 | G | A | upstream_gene_variant | MODIFIER | c.-973G>A| |
S174 S216 |
7 | BAA01g24790 | A01 | 13247682 | C | T | upstream_gene_variant | MODIFIER | c.-183C>T| |
S302 |
8 | BAA01g24790 | A01 | 13247872 | G | A | stop_gained | HIGH | c.8G>A|p.Trp3* |
S38 |
9 | BAA01g24790 | A01 | 13248281 | C | T | synonymous_variant | LOW | c.417C>T|p.Phe139Phe |
S123 S155 S211 |
10 | BAA01g24790 | A01 | 13248578 | C | T | synonymous_variant | LOW | c.714C>T|p.Asp238Asp |
S251 |
11 | BAA01g24790 | A01 | 13248682 | G | A | missense_variant | MODERATE | c.818G>A|p.Arg273Gln |
S287 |
12 | BAA01g24790 | A01 | 13248769 | C | T | missense_variant | MODERATE | c.905C>T|p.Ser302Leu |
S81 S85 |
13 | BAA01g24790 | A01 | 13249213 | C | T | downstream_gene_variant | MODIFIER | c.*329C>T| |
S295 |
14 | BAA01g24790 | A01 | 13249398 | C | T | downstream_gene_variant | MODIFIER | c.*514C>T| |
S205 |
15 | BAA01g24790 | A01 | 13249460 | C | T | downstream_gene_variant | MODIFIER | c.*576C>T| |
S158 |
16 | BAA01g24790 | A01 | 13250036 | C | T | downstream_gene_variant | MODIFIER | c.*1152C>T| |
S166 |
17 | BAA01g24790 | A01 | 13251614 | C | T | downstream_gene_variant | MODIFIER | c.*2730C>T| |
S211 |