Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39990 | A02 | 33802647 | G | A | downstream_gene_variant | MODIFIER | c.*4593C>T| |
S3 |
2 | BAA02g39990 | A02 | 33803389 | C | T | downstream_gene_variant | MODIFIER | c.*3851G>A| |
S79 S91 |
3 | BAA02g39990 | A02 | 33803458 | G | A | downstream_gene_variant | MODIFIER | c.*3782C>T| |
S67 |
4 | BAA02g39990 | A02 | 33805681 | C | T | downstream_gene_variant | MODIFIER | c.*1559G>A| |
S270 |
5 | BAA02g39990 | A02 | 33805823 | G | A | downstream_gene_variant | MODIFIER | c.*1417C>T| |
S191 |
6 | BAA02g39990 | A02 | 33806061 | C | T | downstream_gene_variant | MODIFIER | c.*1179G>A| |
S17 S46 |
7 | BAA02g39990 | A02 | 33807529 | C | T | missense_variant | MODERATE | c.1148G>A|p.Arg383Lys |
S165 |
8 | BAA02g39990 | A02 | 33807553 | C | T | missense_variant | MODERATE | c.1124G>A|p.Gly375Glu |
S255 |
9 | BAA02g39990 | A02 | 33808465 | C | T | missense_variant | MODERATE | c.809G>A|p.Cys270Tyr |
S139 |
10 | BAA02g39990 | A02 | 33808808 | G | A | missense_variant | MODERATE | c.578C>T|p.Thr193Ile |
S45 |
11 | BAA02g39990 | A02 | 33808878 | G | A | synonymous_variant | LOW | c.508C>T|p.Leu170Leu |
S279 |
12 | BAA02g39990 | A02 | 33808946 | C | T | missense_variant | MODERATE | c.440G>A|p.Arg147His |
S152 |
13 | BAA02g39990 | A02 | 33811723 | G | A | upstream_gene_variant | MODIFIER | c.-2338C>T| |
S25 |
14 | BAA02g39990 | A02 | 33811952 | G | A | upstream_gene_variant | MODIFIER | c.-2567C>T| |
S246 |
15 | BAA02g39990 | A02 | 33814242 | C | T | upstream_gene_variant | MODIFIER | c.-4857G>A| |
S121 |