Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26060 | A10 | 20785659 | G | A | upstream_gene_variant | MODIFIER | c.-2343G>A| |
S279 |
2 | BAA10g26060 | A10 | 20786550 | C | T | upstream_gene_variant | MODIFIER | c.-1452C>T| |
S45 |
3 | BAA10g26060 | A10 | 20788182 | G | A | missense_variant | MODERATE | c.181G>A|p.Gly61Arg |
S42 |
4 | BAA10g26060 | A10 | 20788976 | C | T | synonymous_variant | LOW | c.975C>T|p.Leu325Leu |
S117 |
5 | BAA10g26060 | A10 | 20789146 | C | T | missense_variant | MODERATE | c.1145C>T|p.Ser382Leu |
S206 S26 |
6 | BAA10g26060 | A10 | 20789220 | C | T | stop_gained | HIGH | c.1219C>T|p.Gln407* |
S210 S225 |
7 | BAA10g26060 | A10 | 20789260 | C | T | missense_variant | MODERATE | c.1259C>T|p.Ser420Phe |
S144 |
8 | BAA10g26060 | A10 | 20789556 | G | A | missense_variant | MODERATE | c.1555G>A|p.Val519Met |
S100 |
9 | BAA10g26060 | A10 | 20789689 | G | A | missense_variant | MODERATE | c.1688G>A|p.Ser563Asn |
S100 |
10 | BAA10g26060 | A10 | 20789871 | C | T | synonymous_variant | LOW | c.1870C>T|p.Leu624Leu |
S129 |