Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12340 | A10 | 13793369 | G | A | upstream_gene_variant | MODIFIER | c.-3070G>A| |
S171 |
2 | BAA10g12340 | A10 | 13793867 | C | T | upstream_gene_variant | MODIFIER | c.-2572C>T| |
S56 |
3 | BAA10g12340 | A10 | 13796727 | G | A | missense_variant | MODERATE | c.289G>A|p.Ala97Thr |
S267 |
4 | BAA10g12340 | A10 | 13796984 | G | A | synonymous_variant | LOW | c.546G>A|p.Leu182Leu |
S284 |
5 | BAA10g12340 | A10 | 13797391 | C | T | missense_variant | MODERATE | c.953C>T|p.Ser318Phe |
S224 |
6 | BAA10g12340 | A10 | 13797972 | G | A | missense_variant | MODERATE | c.1534G>A|p.Ala512Thr |
S75 S81 |
7 | BAA10g12340 | A10 | 13800440 | C | T | downstream_gene_variant | MODIFIER | c.*1827C>T| |
S187 S243 S298 S299 |
8 | BAA10g12340 | A10 | 13800519 | C | T | downstream_gene_variant | MODIFIER | c.*1906C>T| |
S42 |