Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20690 | A10 | 18492731 | C | T | upstream_gene_variant | MODIFIER | c.-2586C>T| |
S67 |
2 | BAA10g20690 | A10 | 18492872 | C | T | upstream_gene_variant | MODIFIER | c.-2445C>T| |
S168 |
3 | BAA10g20690 | A10 | 18493634 | C | T | upstream_gene_variant | MODIFIER | c.-1683C>T| |
S201 |
4 | BAA10g20690 | A10 | 18494247 | C | T | upstream_gene_variant | MODIFIER | c.-1070C>T| |
S203 |
5 | BAA10g20690 | A10 | 18495556 | C | T | synonymous_variant | LOW | c.240C>T|p.Leu80Leu |
S221 |
6 | BAA10g20690 | A10 | 18495644 | G | A | missense_variant | MODERATE | c.328G>A|p.Glu110Lys |
S240 |
7 | BAA10g20690 | A10 | 18496298 | G | A | missense_variant | MODERATE | c.982G>A|p.Asp328Asn |
S198 |
8 | BAA10g20690 | A10 | 18499463 | G | A | missense_variant | MODERATE | c.2545G>A|p.Glu849Lys |
S39 |
9 | BAA10g20690 | A10 | 18501152 | G | A | stop_gained | HIGH | c.3282G>A|p.Trp1094* |
S198 |
10 | BAA10g20690 | A10 | 18504644 | C | T | downstream_gene_variant | MODIFIER | c.*3438C>T| |
S38 |