Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g58120 | A09 | 57013628 | C | T | missense_variant | MODERATE | c.1513G>A|p.Glu505Lys |
S250 |
2 | BAA09g58120 | A09 | 57013793 | C | T | missense_variant | MODERATE | c.1348G>A|p.Glu450Lys |
S97 |
3 | BAA09g58120 | A09 | 57014117 | G | A | missense_variant | MODERATE | c.1024C>T|p.Pro342Ser |
S288 |
4 | BAA09g58120 | A09 | 57014171 | G | A | missense_variant | MODERATE | c.970C>T|p.Pro324Ser |
S297 |
5 | BAA09g58120 | A09 | 57014426 | C | T | missense_variant | MODERATE | c.715G>A|p.Gly239Arg |
S9 |
6 | BAA09g58120 | A09 | 57015363 | G | A | missense_variant | MODERATE | c.119C>T|p.Ala40Val |
S167 |
7 | BAA09g58120 | A09 | 57019579 | C | T | upstream_gene_variant | MODIFIER | c.-3908G>A| |
S229 |