Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g14700 | A09 | 8385653 | C | T | missense_variant | MODERATE | c.76G>A|p.Ala26Thr |
S156 |
2 | BAA09g14700 | A09 | 8386045 | C | T | upstream_gene_variant | MODIFIER | c.-317G>A| |
S283 |
3 | BAA09g14700 | A09 | 8386831 | C | T | upstream_gene_variant | MODIFIER | c.-1103G>A| |
S196 |
4 | BAA09g14700 | A09 | 8387071 | C | T | upstream_gene_variant | MODIFIER | c.-1343G>A| |
S13 |
5 | BAA09g14700 | A09 | 8388148 | G | A | upstream_gene_variant | MODIFIER | c.-2420C>T| |
S162 |