Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46430 | A02 | 37731551 | G | A | missense_variant | MODERATE | c.1171C>T|p.His391Tyr |
S288 |
2 | BAA02g46430 | A02 | 37732099 | G | A | missense_variant | MODERATE | c.902C>T|p.Pro301Leu |
S211 |
3 | BAA02g46430 | A02 | 37732333 | G | A | synonymous_variant | LOW | c.768C>T|p.Leu256Leu |
S63 S77 S82 |
4 | BAA02g46430 | A02 | 37732767 | G | A | intron_variant | MODIFIER | c.653-319C>T| |
S55 |
5 | BAA02g46430 | A02 | 37736504 | C | T | upstream_gene_variant | MODIFIER | c.-1192G>A| |
S197 |
6 | BAA02g46430 | A02 | 37736861 | G | A | upstream_gene_variant | MODIFIER | c.-1549C>T| |
S162 |
7 | BAA02g46430 | A02 | 37737916 | G | A | upstream_gene_variant | MODIFIER | c.-2604C>T| |
S54 |
8 | BAA02g46430 | A02 | 37739692 | G | A | upstream_gene_variant | MODIFIER | c.-4380C>T| |
S4 |