Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10060 | A02 | 4436636 | G | A | downstream_gene_variant | MODIFIER | c.*2403C>T| |
S52 |
2 | BAA02g10060 | A02 | 4437423 | G | A | downstream_gene_variant | MODIFIER | c.*1616C>T| |
S170 |
3 | BAA02g10060 | A02 | 4439872 | G | A | synonymous_variant | LOW | c.1942C>T|p.Leu648Leu |
S275 |
4 | BAA02g10060 | A02 | 4440125 | G | A | synonymous_variant | LOW | c.1785C>T|p.Ser595Ser |
S126 |
5 | BAA02g10060 | A02 | 4440670 | G | A | missense_variant | MODERATE | c.1406C>T|p.Thr469Ile |
S274 |
6 | BAA02g10060 | A02 | 4441442 | C | T | missense_variant&splice_region_variant | MODERATE | c.937G>A|p.Val313Ile |
S116 |
7 | BAA02g10060 | A02 | 4441581 | G | A | missense_variant | MODERATE | c.908C>T|p.Pro303Leu |
S197 |
8 | BAA02g10060 | A02 | 4441917 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.689-1G>A| |
S119 |
9 | BAA02g10060 | A02 | 4443537 | C | T | upstream_gene_variant | MODIFIER | c.-678G>A| |
S79 S84 |
10 | BAA02g10060 | A02 | 4443788 | G | A | upstream_gene_variant | MODIFIER | c.-929C>T| |
S223 |
11 | BAA02g10060 | A02 | 4445512 | C | T | upstream_gene_variant | MODIFIER | c.-2653G>A| |
S167 |
12 | BAA02g10060 | A02 | 4446035 | G | C | upstream_gene_variant | MODIFIER | c.-3176C>G| |
S193 |
13 | BAA02g10060 | A02 | 4446411 | C | T | upstream_gene_variant | MODIFIER | c.-3552G>A| |
S42 |
14 | BAA02g10060 | A02 | 4446564 | C | T | upstream_gene_variant | MODIFIER | c.-3705G>A| |
S117 |
15 | BAA02g10060 | A02 | 4447190 | C | T | upstream_gene_variant | MODIFIER | c.-4331G>A| |
S189 |