Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22940 | A02 | 12460250 | C | T | upstream_gene_variant | MODIFIER | c.-4695C>T| |
S299 |
2 | BAA02g22940 | A02 | 12460768 | G | A | upstream_gene_variant | MODIFIER | c.-4177G>A| |
S7 |
3 | BAA02g22940 | A02 | 12461711 | G | A | upstream_gene_variant | MODIFIER | c.-3234G>A| |
S13 S140 S168 S279 S64 |
4 | BAA02g22940 | A02 | 12462622 | G | A | upstream_gene_variant | MODIFIER | c.-2323G>A| |
S110 |
5 | BAA02g22940 | A02 | 12463086 | A | T | upstream_gene_variant | MODIFIER | c.-1859A>T| |
S235 |
6 | BAA02g22940 | A02 | 12463509 | G | A | upstream_gene_variant | MODIFIER | c.-1436G>A| |
S143 |
7 | BAA02g22940 | A02 | 12464017 | G | A | upstream_gene_variant | MODIFIER | c.-928G>A| |
S133 |
8 | BAA02g22940 | A02 | 12464590 | G | A | upstream_gene_variant | MODIFIER | c.-355G>A| |
S72 S78 |
9 | BAA02g22940 | A02 | 12465461 | G | A | missense_variant | MODERATE | c.517G>A|p.Glu173Lys |
S109 |
10 | BAA02g22940 | A02 | 12466124 | G | A | missense_variant | MODERATE | c.1180G>A|p.Asp394Asn |
S229 |
11 | BAA02g22940 | A02 | 12466503 | G | A | missense_variant | MODERATE | c.1559G>A|p.Arg520Lys |
S81 S85 |
12 | BAA02g22940 | A02 | 12467090 | C | T | missense_variant | MODERATE | c.1991C>T|p.Thr664Ile |
S32 |
13 | BAA02g22940 | A02 | 12467192 | C | T | missense_variant | MODERATE | c.2093C>T|p.Thr698Ile |
S2 S4 S6 |
14 | BAA02g22940 | A02 | 12467275 | G | A | missense_variant | MODERATE | c.2176G>A|p.Ala726Thr |
S294 |
15 | BAA02g22940 | A02 | 12469876 | G | A | downstream_gene_variant | MODIFIER | c.*691G>A| |
S286 |
16 | BAA02g22940 | A02 | 12470623 | C | T | downstream_gene_variant | MODIFIER | c.*1438C>T| |
S87 |