Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g39850 | A05 | 38777062 | G | A | missense_variant | MODERATE | c.331C>T|p.Pro111Ser |
S181 |
2 | BAA05g39850 | A05 | 38777068 | G | A | missense_variant | MODERATE | c.325C>T|p.Leu109Phe |
S288 |
3 | BAA05g39850 | A05 | 38779091 | C | T | upstream_gene_variant | MODIFIER | c.-1607G>A| |
S162 |
4 | BAA05g39850 | A05 | 38780126 | G | A | upstream_gene_variant | MODIFIER | c.-2642C>T| |
S231 |
5 | BAA05g39850 | A05 | 38781588 | C | T | upstream_gene_variant | MODIFIER | c.-4104G>A| |
S171 |