Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22120 | A10 | 19185985 | C | A | upstream_gene_variant | MODIFIER | c.-572C>A| |
S51 S92 |
2 | BAA10g22120 | A10 | 19189329 | C | T | missense_variant | MODERATE | c.1298C>T|p.Ser433Leu |
S259 |
3 | BAA10g22120 | A10 | 19189877 | G | A | missense_variant | MODERATE | c.1547G>A|p.Gly516Glu |
S174 S27 |
4 | BAA10g22120 | A10 | 19190107 | G | A | missense_variant | MODERATE | c.1690G>A|p.Ala564Thr |
S62 |
5 | BAA10g22120 | A10 | 19190856 | C | T | stop_gained | HIGH | c.1921C>T|p.Gln641* |
S282 |
6 | BAA10g22120 | A10 | 19191259 | C | T | synonymous_variant | LOW | c.2232C>T|p.Phe744Phe |
S191 |