Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05160 | A10 | 2678634 | C | T | upstream_gene_variant | MODIFIER | c.-716C>T| |
S252 |
2 | BAA10g05160 | A10 | 2678720 | G | A | upstream_gene_variant | MODIFIER | c.-630G>A| |
S18 |
3 | BAA10g05160 | A10 | 2678743 | G | A | upstream_gene_variant | MODIFIER | c.-607G>A| |
S277 |
4 | BAA10g05160 | A10 | 2678996 | C | T | upstream_gene_variant | MODIFIER | c.-354C>T| |
S173 |
5 | BAA10g05160 | A10 | 2679893 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.474-1G>A| |
S111 |
6 | BAA10g05160 | A10 | 2680555 | G | A | missense_variant | MODERATE | c.896G>A|p.Arg299Lys |
S171 |
7 | BAA10g05160 | A10 | 2681988 | G | A | missense_variant | MODERATE | c.1753G>A|p.Asp585Asn |
S62 |