Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12440 | A02 | 5587604 | C | T | upstream_gene_variant | MODIFIER | c.-2294C>T| |
S185 |
2 | BAA02g12440 | A02 | 5587728 | C | T | upstream_gene_variant | MODIFIER | c.-2170C>T| |
S212 |
3 | BAA02g12440 | A02 | 5589949 | G | A | missense_variant | MODERATE | c.52G>A|p.Gly18Arg |
S150 |
4 | BAA02g12440 | A02 | 5590535 | C | T | missense_variant | MODERATE | c.350C>T|p.Pro117Leu |
S174 |
5 | BAA02g12440 | A02 | 5591768 | G | A | missense_variant | MODERATE | c.1583G>A|p.Arg528Gln |
S149 |
6 | BAA02g12440 | A02 | 5591930 | C | T | missense_variant | MODERATE | c.1745C>T|p.Pro582Leu |
S267 |
7 | BAA02g12440 | A02 | 5591961 | G | A | synonymous_variant | LOW | c.1776G>A|p.Glu592Glu |
S2 |
8 | BAA02g12440 | A02 | 5592121 | G | A | missense_variant | MODERATE | c.1936G>A|p.Gly646Arg |
S80 |
9 | BAA02g12440 | A02 | 5592314 | C | T | missense_variant | MODERATE | c.2129C>T|p.Ser710Leu |
S128 |
10 | BAA02g12440 | A02 | 5592569 | G | A | missense_variant | MODERATE | c.2384G>A|p.Gly795Glu |
S23 |
11 | BAA02g12440 | A02 | 5592619 | G | A | missense_variant | MODERATE | c.2434G>A|p.Val812Met |
S204 |