Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10060 | A01 | 4545862 | C | T | synonymous_variant | LOW | c.1068G>A|p.Glu356Glu |
S64 |
2 | BAA01g10060 | A01 | 4546638 | C | T | missense_variant | MODERATE | c.551G>A|p.Gly184Glu |
S100 |
3 | BAA01g10060 | A01 | 4547035 | C | T | missense_variant | MODERATE | c.154G>A|p.Ala52Thr |
S107 |
4 | BAA01g10060 | A01 | 4547859 | G | A | upstream_gene_variant | MODIFIER | c.-152C>T| |
S159 S243 |
5 | BAA01g10060 | A01 | 4548349 | G | A | upstream_gene_variant | MODIFIER | c.-642C>T| |
S172 S217 |
6 | BAA01g10060 | A01 | 4550235 | C | T | upstream_gene_variant | MODIFIER | c.-2528G>A| |
S302 |
7 | BAA01g10060 | A01 | 4551342 | C | T | upstream_gene_variant | MODIFIER | c.-3635G>A| |
S166 |
8 | BAA01g10060 | A01 | 4552125 | G | A | upstream_gene_variant | MODIFIER | c.-4418C>T| |
S140 S168 S219 S72 |
9 | BAA01g10060 | A01 | 4552386 | G | A | upstream_gene_variant | MODIFIER | c.-4679C>T| |
S260 |