Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g47580 | A03 | 22858813 | C | T | upstream_gene_variant | MODIFIER | c.-4001C>T| |
S192 |
2 | BAA03g47580 | A03 | 22860282 | C | T | upstream_gene_variant | MODIFIER | c.-2532C>T| |
S161 |
3 | BAA03g47580 | A03 | 22863176 | C | T | synonymous_variant | LOW | c.289C>T|p.Leu97Leu |
S263 |
4 | BAA03g47580 | A03 | 22863558 | C | T | missense_variant | MODERATE | c.671C>T|p.Ala224Val |
S146 |
5 | BAA03g47580 | A03 | 22863793 | C | T | synonymous_variant | LOW | c.906C>T|p.Asn302Asn |
S296 |
6 | BAA03g47580 | A03 | 22864301 | G | A | missense_variant | MODERATE | c.1209G>A|p.Met403Ile |
S59 |
7 | BAA03g47580 | A03 | 22864846 | G | A | missense_variant | MODERATE | c.1754G>A|p.Gly585Asp |
S17 |
8 | BAA03g47580 | A03 | 22865371 | C | T | missense_variant | MODERATE | c.1819C>T|p.Leu607Phe |
S76 |
9 | BAA03g47580 | A03 | 22865417 | G | A | missense_variant | MODERATE | c.1865G>A|p.Gly622Glu |
S36 |