Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00760 | A04 | 410970 | G | A | upstream_gene_variant | MODIFIER | c.-2846G>A| |
S280 |
2 | BAA04g00760 | A04 | 411590 | G | A | upstream_gene_variant | MODIFIER | c.-2226G>A| |
S210 |
3 | BAA04g00760 | A04 | 411792 | C | T | upstream_gene_variant | MODIFIER | c.-2024C>T| |
S200 |
4 | BAA04g00760 | A04 | 411978 | C | T | upstream_gene_variant | MODIFIER | c.-1838C>T| |
S208 |
5 | BAA04g00760 | A04 | 412078 | C | T | upstream_gene_variant | MODIFIER | c.-1738C>T| |
S45 |
6 | BAA04g00760 | A04 | 412420 | G | A | upstream_gene_variant | MODIFIER | c.-1396G>A| |
S82 S92 |
7 | BAA04g00760 | A04 | 414578 | C | T | missense_variant | MODERATE | c.104C>T|p.Ala35Val |
S179 |
8 | BAA04g00760 | A04 | 414894 | G | A | missense_variant | MODERATE | c.334G>A|p.Glu112Lys |
S125 |
9 | BAA04g00760 | A04 | 415559 | G | A | synonymous_variant | LOW | c.801G>A|p.Lys267Lys |
S229 |
10 | BAA04g00760 | A04 | 415695 | G | A | missense_variant | MODERATE | c.937G>A|p.Glu313Lys |
S277 |