Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17500 | A02 | 8716399 | G | A | upstream_gene_variant | MODIFIER | c.-1013G>A| |
S197 |
2 | BAA02g17500 | A02 | 8716492 | C | T | upstream_gene_variant | MODIFIER | c.-920C>T| |
S121 |
3 | BAA02g17500 | A02 | 8716680 | C | T | upstream_gene_variant | MODIFIER | c.-732C>T| |
S25 |
4 | BAA02g17500 | A02 | 8716716 | C | T | upstream_gene_variant | MODIFIER | c.-696C>T| |
S271 |
5 | BAA02g17500 | A02 | 8717230 | C | T | upstream_gene_variant | MODIFIER | c.-182C>T| |
S308 |
6 | BAA02g17500 | A02 | 8717615 | G | A | synonymous_variant | LOW | c.204G>A|p.Arg68Arg |
S132 S215 |
7 | BAA02g17500 | A02 | 8718264 | C | T | missense_variant | MODERATE | c.787C>T|p.Leu263Phe |
S119 |
8 | BAA02g17500 | A02 | 8718292 | C | T | missense_variant | MODERATE | c.815C>T|p.Ser272Phe |
S242 |
9 | BAA02g17500 | A02 | 8719807 | G | A | missense_variant | MODERATE | c.1811G>A|p.Arg604Lys |
S177 |
10 | BAA02g17500 | A02 | 8720218 | G | A | splice_region_variant&intron_variant | LOW | c.2067-6G>A| |
S67 |
11 | BAA02g17500 | A02 | 8723623 | C | T | downstream_gene_variant | MODIFIER | c.*3243C>T| |
S271 |
12 | BAA02g17500 | A02 | 8724033 | C | T | downstream_gene_variant | MODIFIER | c.*3653C>T| |
S272 S302 |
13 | BAA02g17500 | A02 | 8724034 | C | T | downstream_gene_variant | MODIFIER | c.*3654C>T| |
S183 S198 |
14 | BAA02g17500 | A02 | 8725080 | G | A | downstream_gene_variant | MODIFIER | c.*4700G>A| |
S291 |