Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g27990 | A09 | 18382661 | G | A | downstream_gene_variant | MODIFIER | c.*812C>T| |
S233 |
2 | BAA09g27990 | A09 | 18382803 | G | A | downstream_gene_variant | MODIFIER | c.*670C>T| |
S20 |
3 | BAA09g27990 | A09 | 18384357 | G | A | missense_variant | MODERATE | c.2011C>T|p.Pro671Ser |
S129 |
4 | BAA09g27990 | A09 | 18385350 | G | A | synonymous_variant | LOW | c.1353C>T|p.Ile451Ile |
S295 |
5 | BAA09g27990 | A09 | 18386247 | C | T | missense_variant | MODERATE | c.826G>A|p.Val276Met |
S95 |
6 | BAA09g27990 | A09 | 18386531 | C | T | missense_variant | MODERATE | c.661G>A|p.Val221Ile |
S138 S288 |
7 | BAA09g27990 | A09 | 18386866 | C | T | missense_variant | MODERATE | c.544G>A|p.Ala182Thr |
S256 |
8 | BAA09g27990 | A09 | 18387201 | C | T | missense_variant | MODERATE | c.338G>A|p.Gly113Asp |
S272 |
9 | BAA09g27990 | A09 | 18388610 | G | A | upstream_gene_variant | MODIFIER | c.-518C>T| |
S274 |
10 | BAA09g27990 | A09 | 18390499 | C | T | upstream_gene_variant | MODIFIER | c.-2407G>A| |
S111 |
11 | BAA09g27990 | A09 | 18390571 | G | A | upstream_gene_variant | MODIFIER | c.-2479C>T| |
S249 |
12 | BAA09g27990 | A09 | 18390577 | C | T | upstream_gene_variant | MODIFIER | c.-2485G>A| |
S306 S308 |
13 | BAA09g27990 | A09 | 18391489 | C | T | upstream_gene_variant | MODIFIER | c.-3397G>A| |
S227 S75 |
14 | BAA09g27990 | A09 | 18392170 | C | T | upstream_gene_variant | MODIFIER | c.-4078G>A| |
S278 |