Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35920 | A09 | 44213744 | G | A | missense_variant | MODERATE | c.338C>T|p.Thr113Ile |
S207 |
2 | BAA09g35920 | A09 | 44215533 | G | A | upstream_gene_variant | MODIFIER | c.-1452C>T| |
S197 |
3 | BAA09g35920 | A09 | 44216359 | A | C | upstream_gene_variant | MODIFIER | c.-2278T>G| |
S177 |
4 | BAA09g35920 | A09 | 44216870 | G | A | upstream_gene_variant | MODIFIER | c.-2789C>T| |
S72 |
5 | BAA09g35920 | A09 | 44218918 | G | A | upstream_gene_variant | MODIFIER | c.-4837C>T| |
S221 |