Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g46450 | A03 | 22247213 | C | T | missense_variant | MODERATE | c.2681G>A|p.Arg894Lys |
S190 |
2 | BAA03g46450 | A03 | 22247626 | G | A | missense_variant | MODERATE | c.2399C>T|p.Ala800Val |
S166 |
3 | BAA03g46450 | A03 | 22247877 | C | T | missense_variant | MODERATE | c.2243G>A|p.Gly748Glu |
S228 |
4 | BAA03g46450 | A03 | 22249093 | G | A | missense_variant | MODERATE | c.1549C>T|p.Pro517Ser |
S167 |
5 | BAA03g46450 | A03 | 22250290 | G | A | missense_variant | MODERATE | c.772C>T|p.Leu258Phe |
S277 |
6 | BAA03g46450 | A03 | 22250444 | C | T | stop_gained | HIGH | c.618G>A|p.Trp206* |
S87 |
7 | BAA03g46450 | A03 | 22251007 | G | A | missense_variant | MODERATE | c.232C>T|p.Pro78Ser |
S136 |
8 | BAA03g46450 | A03 | 22251730 | G | A | upstream_gene_variant | MODIFIER | c.-492C>T| |
S177 |
9 | BAA03g46450 | A03 | 22255710 | C | T | upstream_gene_variant | MODIFIER | c.-4472G>A| |
S19 |