Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27450 | A02 | 15450711 | C | T | synonymous_variant | LOW | c.1680G>A|p.Gln560Gln |
S46 |
2 | BAA02g27450 | A02 | 15450829 | G | A | missense_variant | MODERATE | c.1562C>T|p.Pro521Leu |
S143 |
3 | BAA02g27450 | A02 | 15451310 | G | A | missense_variant | MODERATE | c.1081C>T|p.Leu361Phe |
S241 |
4 | BAA02g27450 | A02 | 15451328 | C | T | missense_variant | MODERATE | c.1063G>A|p.Gly355Ser |
S77 S82 |
5 | BAA02g27450 | A02 | 15451565 | C | T | missense_variant | MODERATE | c.826G>A|p.Val276Ile |
S179 |
6 | BAA02g27450 | A02 | 15451605 | G | A | synonymous_variant | LOW | c.786C>T|p.Phe262Phe |
S50 |
7 | BAA02g27450 | A02 | 15451675 | C | T | missense_variant | MODERATE | c.716G>A|p.Arg239Lys |
S167 |
8 | BAA02g27450 | A02 | 15452317 | G | A | missense_variant | MODERATE | c.239C>T|p.Ala80Val |
S223 |
9 | BAA02g27450 | A02 | 15452454 | G | A | synonymous_variant | LOW | c.102C>T|p.Phe34Phe |
S184 |
10 | BAA02g27450 | A02 | 15453549 | G | A | upstream_gene_variant | MODIFIER | c.-994C>T| |
S19 |
11 | BAA02g27450 | A02 | 15453580 | G | A | upstream_gene_variant | MODIFIER | c.-1025C>T| |
S197 |
12 | BAA02g27450 | A02 | 15454442 | G | A | upstream_gene_variant | MODIFIER | c.-1887C>T| |
S67 |
13 | BAA02g27450 | A02 | 15455034 | G | A | upstream_gene_variant | MODIFIER | c.-2479C>T| |
S265 |