Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46580 | A09 | 51262514 | C | T | missense_variant | MODERATE | c.715G>A|p.Gly239Arg |
S108 |
2 | BAA09g46580 | A09 | 51263009 | C | T | synonymous_variant | LOW | c.297G>A|p.Gly99Gly |
S296 |
3 | BAA09g46580 | A09 | 51263194 | G | A | missense_variant | MODERATE | c.214C>T|p.Arg72Trp |
S69 |
4 | BAA09g46580 | A09 | 51263688 | G | A | upstream_gene_variant | MODIFIER | c.-281C>T| |
S246 |
5 | BAA09g46580 | A09 | 51264819 | G | A | upstream_gene_variant | MODIFIER | c.-1412C>T| |
S1 S90 |
6 | BAA09g46580 | A09 | 51265880 | C | T | upstream_gene_variant | MODIFIER | c.-2473G>A| |
S163 |