Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16460 | A02 | 8031389 | G | A | missense_variant | MODERATE | c.211C>T|p.Pro71Ser |
S274 |
2 | BAA02g16460 | A02 | 8031545 | G | A | missense_variant | MODERATE | c.55C>T|p.Leu19Phe |
S7 |
3 | BAA02g16460 | A02 | 8031903 | G | A | upstream_gene_variant | MODIFIER | c.-304C>T| |
S246 |
4 | BAA02g16460 | A02 | 8032089 | G | A | upstream_gene_variant | MODIFIER | c.-490C>T| |
S161 |
5 | BAA02g16460 | A02 | 8032538 | C | T | upstream_gene_variant | MODIFIER | c.-939G>A| |
S84 S93 |
6 | BAA02g16460 | A02 | 8034743 | C | T | upstream_gene_variant | MODIFIER | c.-3144G>A| |
S124 |