Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g13450 | A05 | 6972854 | C | T | missense_variant | MODERATE | c.1147G>A|p.Ala383Thr |
S16 |
2 | BAA05g13450 | A05 | 6973861 | G | A | synonymous_variant | LOW | c.297C>T|p.Phe99Phe |
S294 |
3 | BAA05g13450 | A05 | 6974030 | G | A | missense_variant | MODERATE | c.128C>T|p.Ser43Phe |
S280 |
4 | BAA05g13450 | A05 | 6974269 | C | T | upstream_gene_variant | MODIFIER | c.-112G>A| |
S195 |
5 | BAA05g13450 | A05 | 6974314 | G | A | upstream_gene_variant | MODIFIER | c.-157C>T| |
S161 |
6 | BAA05g13450 | A05 | 6974459 | C | T | upstream_gene_variant | MODIFIER | c.-302G>A| |
S291 |
7 | BAA05g13450 | A05 | 6975359 | T | A | upstream_gene_variant | MODIFIER | c.-1202A>T| |
S136 |
8 | BAA05g13450 | A05 | 6975980 | T | A | upstream_gene_variant | MODIFIER | c.-1823A>T| |
S203 |
9 | BAA05g13450 | A05 | 6976039 | G | A | upstream_gene_variant | MODIFIER | c.-1882C>T| |
S77 S82 |