Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02690 | A01 | 1239418 | C | T | upstream_gene_variant | MODIFIER | c.-4928C>T| |
S2 |
2 | BAA01g02690 | A01 | 1239450 | C | T | upstream_gene_variant | MODIFIER | c.-4896C>T| |
S19 |
3 | BAA01g02690 | A01 | 1241572 | G | T | upstream_gene_variant | MODIFIER | c.-2774G>T| |
S200 |
4 | BAA01g02690 | A01 | 1242738 | C | T | upstream_gene_variant | MODIFIER | c.-1608C>T| |
S64 |
5 | BAA01g02690 | A01 | 1245151 | G | A | intron_variant | MODIFIER | c.441+270G>A| |
S197 |
6 | BAA01g02690 | A01 | 1246246 | G | A | missense_variant | MODERATE | c.1031G>A|p.Ser344Asn |
S177 |
7 | BAA01g02690 | A01 | 1247270 | C | T | downstream_gene_variant | MODIFIER | c.*939C>T| |
S30 S31 |
8 | BAA01g02690 | A01 | 1247567 | C | T | downstream_gene_variant | MODIFIER | c.*1236C>T| |
S61 |
9 | BAA01g02690 | A01 | 1248598 | G | A | downstream_gene_variant | MODIFIER | c.*2267G>A| |
S247 |