Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27120 | A02 | 15228367 | G | A | upstream_gene_variant | MODIFIER | c.-2359G>A| |
S68 |
2 | BAA02g27120 | A02 | 15228487 | G | A | upstream_gene_variant | MODIFIER | c.-2239G>A| |
S280 |
3 | BAA02g27120 | A02 | 15229661 | C | T | upstream_gene_variant | MODIFIER | c.-1065C>T| |
S167 |
4 | BAA02g27120 | A02 | 15230271 | C | T | upstream_gene_variant | MODIFIER | c.-455C>T| |
S273 |
5 | BAA02g27120 | A02 | 15231024 | C | T | synonymous_variant | LOW | c.229C>T|p.Leu77Leu |
S168 |
6 | BAA02g27120 | A02 | 15231682 | G | A | intron_variant | MODIFIER | c.765+39G>A| |
S59 |
7 | BAA02g27120 | A02 | 15233280 | G | A | missense_variant | MODERATE | c.1717G>A|p.Glu573Lys |
S12 |
8 | BAA02g27120 | A02 | 15233371 | C | T | missense_variant | MODERATE | c.1808C>T|p.Pro603Leu |
S282 |
9 | BAA02g27120 | A02 | 15234762 | C | T | missense_variant | MODERATE | c.2888C>T|p.Ser963Phe |
S270 |
10 | BAA02g27120 | A02 | 15234931 | C | T | synonymous_variant | LOW | c.3057C>T|p.Ile1019Ile |
S261 |
11 | BAA02g27120 | A02 | 15235011 | G | A | missense_variant | MODERATE | c.3070G>A|p.Val1024Met |
S146 |
12 | BAA02g27120 | A02 | 15235710 | C | T | synonymous_variant | LOW | c.3567C>T|p.Arg1189Arg |
S267 |