Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49030 | A09 | 52598906 | C | T | upstream_gene_variant | MODIFIER | c.-988C>T| |
S138 |
2 | BAA09g49030 | A09 | 52599071 | C | T | upstream_gene_variant | MODIFIER | c.-823C>T| |
S224 |
3 | BAA09g49030 | A09 | 52600120 | C | T | missense_variant | MODERATE | c.227C>T|p.Ser76Phe |
S138 |
4 | BAA09g49030 | A09 | 52600209 | G | A | missense_variant | MODERATE | c.316G>A|p.Glu106Lys |
S308 |
5 | BAA09g49030 | A09 | 52600360 | G | A | missense_variant | MODERATE | c.467G>A|p.Arg156Lys |
S202 |
6 | BAA09g49030 | A09 | 52600913 | G | A | splice_region_variant&synonymous_variant | LOW | c.825G>A|p.Arg275Arg |
S70 |