Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18600 | A09 | 11149032 | G | A | upstream_gene_variant | MODIFIER | c.-966G>A| |
S197 |
2 | BAA09g18600 | A09 | 11149489 | G | A | upstream_gene_variant | MODIFIER | c.-509G>A| |
S298 |
3 | BAA09g18600 | A09 | 11152318 | G | A | missense_variant | MODERATE | c.2321G>A|p.Ser774Asn |
S129 |
4 | BAA09g18600 | A09 | 11152519 | C | T | missense_variant | MODERATE | c.2522C>T|p.Pro841Leu |
S292 |
5 | BAA09g18600 | A09 | 11154825 | C | T | downstream_gene_variant | MODIFIER | c.*745C>T| |
S168 |
6 | BAA09g18600 | A09 | 11156371 | C | T | downstream_gene_variant | MODIFIER | c.*2291C>T| |
S242 |
7 | BAA09g18600 | A09 | 11156914 | G | A | downstream_gene_variant | MODIFIER | c.*2834G>A| |
S113 |
8 | BAA09g18600 | A09 | 11157262 | G | A | downstream_gene_variant | MODIFIER | c.*3182G>A| |
S40 S49 |
9 | BAA09g18600 | A09 | 11157588 | G | A | downstream_gene_variant | MODIFIER | c.*3508G>A| |
S291 |