Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20780 | A10 | 18532229 | C | T | missense_variant | MODERATE | c.1475G>A|p.Gly492Asp |
S173 |
2 | BAA10g20780 | A10 | 18532361 | G | T | missense_variant | MODERATE | c.1343C>A|p.Ala448Glu |
S61 |
3 | BAA10g20780 | A10 | 18532892 | C | T | missense_variant | MODERATE | c.812G>A|p.Gly271Glu |
S133 |
4 | BAA10g20780 | A10 | 18533801 | C | T | upstream_gene_variant | MODIFIER | c.-98G>A| |
S125 |
5 | BAA10g20780 | A10 | 18533852 | G | A | upstream_gene_variant | MODIFIER | c.-149C>T| |
S118 |
6 | BAA10g20780 | A10 | 18533948 | G | A | upstream_gene_variant | MODIFIER | c.-245C>T| |
S128 |
7 | BAA10g20780 | A10 | 18535425 | C | T | upstream_gene_variant | MODIFIER | c.-1722G>A| |
S199 |
8 | BAA10g20780 | A10 | 18536724 | C | T | upstream_gene_variant | MODIFIER | c.-3021G>A| |
S183 |