Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46620 | A02 | 37852050 | G | A | upstream_gene_variant | MODIFIER | c.-2342G>A| |
S36 |
2 | BAA02g46620 | A02 | 37852539 | G | A | upstream_gene_variant | MODIFIER | c.-1853G>A| |
S130 |
3 | BAA02g46620 | A02 | 37852549 | C | T | upstream_gene_variant | MODIFIER | c.-1843C>T| |
S71 |
4 | BAA02g46620 | A02 | 37852608 | G | A | upstream_gene_variant | MODIFIER | c.-1784G>A| |
S156 |
5 | BAA02g46620 | A02 | 37854413 | C | T | missense_variant | MODERATE | c.22C>T|p.Pro8Ser |
S6 |
6 | BAA02g46620 | A02 | 37854579 | C | T | missense_variant | MODERATE | c.188C>T|p.Ser63Phe |
S206 S26 |
7 | BAA02g46620 | A02 | 37854653 | C | T | synonymous_variant | LOW | c.262C>T|p.Leu88Leu |
S295 |
8 | BAA02g46620 | A02 | 37855505 | C | T | missense_variant | MODERATE | c.782C>T|p.Ala261Val |
S262 |
9 | BAA02g46620 | A02 | 37857192 | C | T | synonymous_variant | LOW | c.1480C>T|p.Leu494Leu |
S231 |
10 | BAA02g46620 | A02 | 37859781 | G | A | missense_variant | MODERATE | c.2686G>A|p.Glu896Lys |
S13 |
11 | BAA02g46620 | A02 | 37862836 | G | A | downstream_gene_variant | MODIFIER | c.*2975G>A| |
S292 |