Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08350 | A02 | 3574985 | C | T | splice_region_variant&intron_variant | LOW | c.2475+5G>A| |
S159 S188 S276 S298 S299 |
2 | BAA02g08350 | A02 | 3575064 | G | A | missense_variant | MODERATE | c.2401C>T|p.Arg801Trp |
S52 |
3 | BAA02g08350 | A02 | 3575895 | G | A | synonymous_variant | LOW | c.1869C>T|p.Pro623Pro |
S260 |
4 | BAA02g08350 | A02 | 3575913 | G | A | splice_region_variant&intron_variant | LOW | c.1856-5C>T| |
S127 |
5 | BAA02g08350 | A02 | 3578210 | G | A | splice_region_variant&intron_variant | LOW | c.622-4C>T| |
S105 S106 |
6 | BAA02g08350 | A02 | 3579574 | C | T | upstream_gene_variant | MODIFIER | c.-305G>A| |
S226 |
7 | BAA02g08350 | A02 | 3580043 | G | A | upstream_gene_variant | MODIFIER | c.-774C>T| |
S209 |
8 | BAA02g08350 | A02 | 3580530 | G | A | upstream_gene_variant | MODIFIER | c.-1261C>T| |
S110 |
9 | BAA02g08350 | A02 | 3581283 | G | A | upstream_gene_variant | MODIFIER | c.-2014C>T| |
S198 |
10 | BAA02g08350 | A02 | 3583949 | C | T | upstream_gene_variant | MODIFIER | c.-4680G>A| |
S171 |