Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g21060 | A08 | 16067822 | C | T | upstream_gene_variant | MODIFIER | c.-4087C>T| |
S139 |
2 | BAA08g21060 | A08 | 16067869 | C | T | upstream_gene_variant | MODIFIER | c.-4040C>T| |
S175 |
3 | BAA08g21060 | A08 | 16071979 | C | T | missense_variant | MODERATE | c.71C>T|p.Thr24Ile |
S178 |
4 | BAA08g21060 | A08 | 16073400 | G | A | missense_variant | MODERATE | c.679G>A|p.Gly227Ser |
S202 |