Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20900 | A09 | 12944698 | G | A | missense_variant | MODERATE | c.455C>T|p.Ala152Val |
S192 |
2 | BAA09g20900 | A09 | 12946031 | C | T | upstream_gene_variant | MODIFIER | c.-398G>A| |
S18 |
3 | BAA09g20900 | A09 | 12946174 | C | T | upstream_gene_variant | MODIFIER | c.-541G>A| |
S187 |
4 | BAA09g20900 | A09 | 12946208 | C | T | upstream_gene_variant | MODIFIER | c.-575G>A| |
S117 |
5 | BAA09g20900 | A09 | 12947950 | G | A | upstream_gene_variant | MODIFIER | c.-2317C>T| |
S196 |
6 | BAA09g20900 | A09 | 12948302 | G | A | upstream_gene_variant | MODIFIER | c.-2669C>T| |
S281 S282 |
7 | BAA09g20900 | A09 | 12948948 | G | A | upstream_gene_variant | MODIFIER | c.-3315C>T| |
S40 S49 |
8 | BAA09g20900 | A09 | 12949709 | G | A | upstream_gene_variant | MODIFIER | c.-4076C>T| |
S209 |