Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g24700 | A09 | 15846313 | G | A | upstream_gene_variant | MODIFIER | c.-2802G>A| |
S233 |
2 | BAA09g24700 | A09 | 15846394 | C | T | upstream_gene_variant | MODIFIER | c.-2721C>T| |
S284 |
3 | BAA09g24700 | A09 | 15846772 | G | A | upstream_gene_variant | MODIFIER | c.-2343G>A| |
S292 |
4 | BAA09g24700 | A09 | 15847310 | G | A | upstream_gene_variant | MODIFIER | c.-1805G>A| |
S166 |
5 | BAA09g24700 | A09 | 15848548 | G | A | upstream_gene_variant | MODIFIER | c.-567G>A| |
S74 |
6 | BAA09g24700 | A09 | 15849343 | G | A | missense_variant | MODERATE | c.229G>A|p.Glu77Lys |
S289 |
7 | BAA09g24700 | A09 | 15850046 | C | T | missense_variant | MODERATE | c.725C>T|p.Pro242Leu |
S36 |
8 | BAA09g24700 | A09 | 15850124 | C | T | missense_variant | MODERATE | c.803C>T|p.Ser268Phe |
S28 |
9 | BAA09g24700 | A09 | 15850177 | C | T | missense_variant | MODERATE | c.856C>T|p.Leu286Phe |
S228 |
10 | BAA09g24700 | A09 | 15850273 | C | T | missense_variant | MODERATE | c.952C>T|p.Pro318Ser |
S19 |