Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20140 | A10 | 18239796 | C | T | missense_variant&splice_region_variant | MODERATE | c.1010G>A|p.Gly337Glu |
S187 |
2 | BAA10g20140 | A10 | 18239931 | C | T | missense_variant | MODERATE | c.875G>A|p.Arg292Lys |
S124 |
3 | BAA10g20140 | A10 | 18240795 | C | T | missense_variant | MODERATE | c.454G>A|p.Gly152Ser |
S25 |
4 | BAA10g20140 | A10 | 18240834 | C | T | missense_variant | MODERATE | c.415G>A|p.Glu139Lys |
S244 |
5 | BAA10g20140 | A10 | 18241852 | C | T | upstream_gene_variant | MODIFIER | c.-604G>A| |
S206 |
6 | BAA10g20140 | A10 | 18243212 | C | T | upstream_gene_variant | MODIFIER | c.-1964G>A| |
S18 |
7 | BAA10g20140 | A10 | 18245798 | A | G | upstream_gene_variant | MODIFIER | c.-4550T>C| |
S168 |