Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g15820 | A03 | 6772491 | C | T | upstream_gene_variant | MODIFIER | c.-2462C>T| |
S182 |
2 | BAA03g15820 | A03 | 6772527 | C | T | upstream_gene_variant | MODIFIER | c.-2426C>T| |
S44 |
3 | BAA03g15820 | A03 | 6772608 | C | T | upstream_gene_variant | MODIFIER | c.-2345C>T| |
S260 |
4 | BAA03g15820 | A03 | 6772805 | G | A | upstream_gene_variant | MODIFIER | c.-2148G>A| |
S149 |
5 | BAA03g15820 | A03 | 6773131 | G | A | upstream_gene_variant | MODIFIER | c.-1822G>A| |
S270 |
6 | BAA03g15820 | A03 | 6773552 | G | A | upstream_gene_variant | MODIFIER | c.-1401G>A| |
S274 |
7 | BAA03g15820 | A03 | 6774685 | C | T | upstream_gene_variant | MODIFIER | c.-268C>T| |
S207 |
8 | BAA03g15820 | A03 | 6775180 | C | T | synonymous_variant | LOW | c.228C>T|p.Asp76Asp |
S279 |
9 | BAA03g15820 | A03 | 6775554 | C | T | missense_variant | MODERATE | c.526C>T|p.Leu176Phe |
S59 |