Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g43980 | A09 | 49881962 | C | T | upstream_gene_variant | MODIFIER | c.-2635C>T| |
S269 |
2 | BAA09g43980 | A09 | 49884070 | G | A | upstream_gene_variant | MODIFIER | c.-527G>A| |
S149 |
3 | BAA09g43980 | A09 | 49884186 | C | T | upstream_gene_variant | MODIFIER | c.-411C>T| |
S66 |
4 | BAA09g43980 | A09 | 49884375 | G | A | upstream_gene_variant | MODIFIER | c.-222G>A| |
S244 |
5 | BAA09g43980 | A09 | 49885808 | C | T | missense_variant | MODERATE | c.385C>T|p.Leu129Phe |
S219 S72 |
6 | BAA09g43980 | A09 | 49885843 | C | T | splice_region_variant&intron_variant | LOW | c.414+6C>T| |
S224 |
7 | BAA09g43980 | A09 | 49886245 | G | A | missense_variant | MODERATE | c.709G>A|p.Asp237Asn |
S233 |