Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18120 | A10 | 17113874 | G | A | upstream_gene_variant | MODIFIER | c.-4897G>A| |
S16 |
2 | BAA10g18120 | A10 | 17116730 | C | T | upstream_gene_variant | MODIFIER | c.-2041C>T| |
S256 |
3 | BAA10g18120 | A10 | 17117204 | G | A | upstream_gene_variant | MODIFIER | c.-1567G>A| |
S198 |
4 | BAA10g18120 | A10 | 17117711 | C | T | upstream_gene_variant | MODIFIER | c.-1060C>T| |
S204 |
5 | BAA10g18120 | A10 | 17117763 | C | T | upstream_gene_variant | MODIFIER | c.-1008C>T| |
S260 |
6 | BAA10g18120 | A10 | 17118088 | C | T | upstream_gene_variant | MODIFIER | c.-683C>T| |
S286 |
7 | BAA10g18120 | A10 | 17118417 | G | A | upstream_gene_variant | MODIFIER | c.-354G>A| |
S175 |
8 | BAA10g18120 | A10 | 17118555 | C | T | upstream_gene_variant | MODIFIER | c.-216C>T| |
S113 |
9 | BAA10g18120 | A10 | 17119391 | C | T | synonymous_variant | LOW | c.621C>T|p.Thr207Thr |
S306 |
10 | BAA10g18120 | A10 | 17119471 | C | T | missense_variant | MODERATE | c.701C>T|p.Pro234Leu |
S188 |
11 | BAA10g18120 | A10 | 17119555 | C | T | missense_variant | MODERATE | c.785C>T|p.Ser262Phe |
S26 |