Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g18440 | A04 | 22269679 | C | T | missense_variant | MODERATE | c.22G>A|p.Ala8Thr |
S267 |
2 | BAA04g18440 | A04 | 22269733 | C | T | upstream_gene_variant | MODIFIER | c.-33G>A| |
S255 |
3 | BAA04g18440 | A04 | 22270215 | C | T | upstream_gene_variant | MODIFIER | c.-515G>A| |
S267 |
4 | BAA04g18440 | A04 | 22270487 | G | A | upstream_gene_variant | MODIFIER | c.-787C>T| |
S155 |
5 | BAA04g18440 | A04 | 22270674 | C | T | upstream_gene_variant | MODIFIER | c.-974G>A| |
S110 |
6 | BAA04g18440 | A04 | 22270849 | C | T | upstream_gene_variant | MODIFIER | c.-1149G>A| |
S128 |
7 | BAA04g18440 | A04 | 22273754 | G | A | upstream_gene_variant | MODIFIER | c.-4054C>T| |
S280 |
8 | BAA04g18440 | A04 | 22273870 | G | A | upstream_gene_variant | MODIFIER | c.-4170C>T| |
S169 |
9 | BAA04g18440 | A04 | 22274194 | G | A | upstream_gene_variant | MODIFIER | c.-4494C>T| |
S262 |
10 | BAA04g18440 | A04 | 22274333 | G | A | upstream_gene_variant | MODIFIER | c.-4633C>T| |
S208 S93 |