Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26220 | A01 | 14567151 | C | T | upstream_gene_variant | MODIFIER | c.-3551C>T| |
S99 |
2 | BAA01g26220 | A01 | 14567470 | G | A | upstream_gene_variant | MODIFIER | c.-3232G>A| |
S308 |
3 | BAA01g26220 | A01 | 14567725 | G | A | upstream_gene_variant | MODIFIER | c.-2977G>A| |
S152 |
4 | BAA01g26220 | A01 | 14568697 | G | A | upstream_gene_variant | MODIFIER | c.-2005G>A| |
S244 |
5 | BAA01g26220 | A01 | 14568854 | G | A | upstream_gene_variant | MODIFIER | c.-1848G>A| |
S257 |
6 | BAA01g26220 | A01 | 14569893 | C | T | upstream_gene_variant | MODIFIER | c.-809C>T| |
S130 |
7 | BAA01g26220 | A01 | 14571122 | C | T | stop_gained | HIGH | c.343C>T|p.Gln115* |
S270 |
8 | BAA01g26220 | A01 | 14571127 | G | A | synonymous_variant | LOW | c.348G>A|p.Arg116Arg |
S110 |
9 | BAA01g26220 | A01 | 14571504 | C | T | missense_variant | MODERATE | c.725C>T|p.Ala242Val |
S104 S52 |
10 | BAA01g26220 | A01 | 14573657 | C | T | downstream_gene_variant | MODIFIER | c.*899C>T| |
S256 |
11 | BAA01g26220 | A01 | 14573669 | G | A | downstream_gene_variant | MODIFIER | c.*911G>A| |
S13 S140 S168 S219 S279 |