Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19610 | A02 | 10193731 | G | A | downstream_gene_variant | MODIFIER | c.*4996C>T| |
S19 |
2 | BAA02g19610 | A02 | 10193884 | C | T | downstream_gene_variant | MODIFIER | c.*4843G>A| |
S163 |
3 | BAA02g19610 | A02 | 10195084 | G | A | downstream_gene_variant | MODIFIER | c.*3643C>T| |
S187 |
4 | BAA02g19610 | A02 | 10197593 | C | T | downstream_gene_variant | MODIFIER | c.*1134G>A| |
S52 |
5 | BAA02g19610 | A02 | 10197937 | C | T | downstream_gene_variant | MODIFIER | c.*790G>A| |
S67 |
6 | BAA02g19610 | A02 | 10198157 | C | T | downstream_gene_variant | MODIFIER | c.*570G>A| |
S249 |
7 | BAA02g19610 | A02 | 10198723 | G | A | downstream_gene_variant | MODIFIER | c.*4C>T| |
S155 |
8 | BAA02g19610 | A02 | 10199229 | C | T | synonymous_variant | LOW | c.900G>A|p.Gln300Gln |
S185 |
9 | BAA02g19610 | A02 | 10199338 | G | A | intron_variant | MODIFIER | c.803-12C>T| |
S13 |
10 | BAA02g19610 | A02 | 10199819 | G | A | intron_variant | MODIFIER | c.553-10C>T| |
S134 |
11 | BAA02g19610 | A02 | 10200011 | G | A | missense_variant | MODERATE | c.421C>T|p.Pro141Ser |
S288 |
12 | BAA02g19610 | A02 | 10200567 | C | T | upstream_gene_variant | MODIFIER | c.-55G>A| |
S88 |
13 | BAA02g19610 | A02 | 10204680 | G | A | upstream_gene_variant | MODIFIER | c.-4168C>T| |
S168 |
14 | BAA02g19610 | A02 | 10204993 | C | T | upstream_gene_variant | MODIFIER | c.-4481G>A| |
S233 |