Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19060 | A10 | 17618659 | G | A | upstream_gene_variant | MODIFIER | c.-3521G>A| |
S192 |
2 | BAA10g19060 | A10 | 17620091 | G | A | upstream_gene_variant | MODIFIER | c.-2089G>A| |
S180 |
3 | BAA10g19060 | A10 | 17621660 | C | T | upstream_gene_variant | MODIFIER | c.-520C>T| |
S46 |
4 | BAA10g19060 | A10 | 17621854 | C | T | upstream_gene_variant | MODIFIER | c.-326C>T| |
S5 |
5 | BAA10g19060 | A10 | 17623119 | C | T | missense_variant | MODERATE | c.940C>T|p.Pro314Ser |
S110 |
6 | BAA10g19060 | A10 | 17623445 | C | T | synonymous_variant | LOW | c.1266C>T|p.Leu422Leu |
S203 |
7 | BAA10g19060 | A10 | 17623732 | G | A | missense_variant | MODERATE | c.1553G>A|p.Gly518Asp |
S65 |
8 | BAA10g19060 | A10 | 17624214 | C | T | missense_variant | MODERATE | c.2035C>T|p.Pro679Ser |
S40 |