Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28080 | A02 | 15806855 | G | A | missense_variant | MODERATE | c.29G>A|p.Arg10Lys |
S286 |
2 | BAA02g28080 | A02 | 15806912 | C | T | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S252 |
3 | BAA02g28080 | A02 | 15807462 | G | A | missense_variant | MODERATE | c.548G>A|p.Arg183Lys |
S97 |
4 | BAA02g28080 | A02 | 15807482 | G | A | splice_donor_variant&intron_variant | HIGH | c.567+1G>A| |
S10 S297 |
5 | BAA02g28080 | A02 | 15807948 | C | T | synonymous_variant | LOW | c.954C>T|p.Leu318Leu |
S180 |
6 | BAA02g28080 | A02 | 15808001 | C | T | missense_variant | MODERATE | c.1007C>T|p.Thr336Ile |
S2 |
7 | BAA02g28080 | A02 | 15808659 | C | T | missense_variant | MODERATE | c.1576C>T|p.Arg526Cys |
S51 |
8 | BAA02g28080 | A02 | 15808905 | C | T | missense_variant | MODERATE | c.1822C>T|p.Leu608Phe |
S178 |
9 | BAA02g28080 | A02 | 15809197 | G | A | downstream_gene_variant | MODIFIER | c.*92G>A| |
S237 |
10 | BAA02g28080 | A02 | 15811787 | G | A | downstream_gene_variant | MODIFIER | c.*2682G>A| |
S225 S73 |