Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19010 | A05 | 11066244 | G | A | upstream_gene_variant | MODIFIER | c.-3753G>A| |
S125 |
2 | BAA05g19010 | A05 | 11066522 | G | A | upstream_gene_variant | MODIFIER | c.-3475G>A| |
S18 S221 S293 |
3 | BAA05g19010 | A05 | 11070048 | G | A | missense_variant | MODERATE | c.52G>A|p.Ala18Thr |
S159 |
4 | BAA05g19010 | A05 | 11070322 | C | T | missense_variant | MODERATE | c.235C>T|p.Leu79Phe |
S289 S290 |
5 | BAA05g19010 | A05 | 11071288 | C | T | missense_variant | MODERATE | c.685C>T|p.Arg229Cys |
S164 |
6 | BAA05g19010 | A05 | 11071923 | C | T | synonymous_variant | LOW | c.1077C>T|p.Phe359Phe |
S167 |
7 | BAA05g19010 | A05 | 11074255 | C | T | downstream_gene_variant | MODIFIER | c.*2137C>T| |
S207 |
8 | BAA05g19010 | A05 | 11074920 | G | A | downstream_gene_variant | MODIFIER | c.*2802G>A| |
S208 S219 |
9 | BAA05g19010 | A05 | 11076694 | C | T | downstream_gene_variant | MODIFIER | c.*4576C>T| |
S53 |
10 | BAA05g19010 | A05 | 11076700 | C | T | downstream_gene_variant | MODIFIER | c.*4582C>T| |
S106 |