Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15770 | A10 | 15992884 | T | A | synonymous_variant | LOW | c.45T>A|p.Ser15Ser |
S296 |
2 | BAA10g15770 | A10 | 15993337 | G | A | missense_variant | MODERATE | c.260G>A|p.Gly87Glu |
S184 |
3 | BAA10g15770 | A10 | 15993580 | G | A | missense_variant | MODERATE | c.394G>A|p.Glu132Lys |
S9 |
4 | BAA10g15770 | A10 | 15994117 | G | A | stop_gained | HIGH | c.704G>A|p.Trp235* |
S65 |
5 | BAA10g15770 | A10 | 15998759 | G | A | downstream_gene_variant | MODIFIER | c.*4356G>A| |
S155 S211 |