Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26120 | A10 | 20820964 | G | A | synonymous_variant | LOW | c.1938C>T|p.Pro646Pro |
S197 |
2 | BAA10g26120 | A10 | 20821926 | G | A | missense_variant | MODERATE | c.976C>T|p.Pro326Ser |
S127 |
3 | BAA10g26120 | A10 | 20821936 | G | A | synonymous_variant | LOW | c.966C>T|p.Arg322Arg |
S128 |
4 | BAA10g26120 | A10 | 20822486 | G | A | missense_variant | MODERATE | c.416C>T|p.Ser139Phe |
S128 |
5 | BAA10g26120 | A10 | 20823203 | G | A | upstream_gene_variant | MODIFIER | c.-302C>T| |
S112 |
6 | BAA10g26120 | A10 | 20825442 | C | T | upstream_gene_variant | MODIFIER | c.-2541G>A| |
S107 |