Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46320 | A02 | 37686871 | C | T | missense_variant | MODERATE | c.1019G>A|p.Arg340Gln |
S177 |
2 | BAA02g46320 | A02 | 37687064 | G | A | missense_variant | MODERATE | c.826C>T|p.Leu276Phe |
S36 |
3 | BAA02g46320 | A02 | 37687307 | G | A | missense_variant | MODERATE | c.583C>T|p.Pro195Ser |
S276 |
4 | BAA02g46320 | A02 | 37687634 | G | A | missense_variant | MODERATE | c.256C>T|p.Leu86Phe |
S251 |
5 | BAA02g46320 | A02 | 37687688 | G | A | missense_variant | MODERATE | c.202C>T|p.Leu68Phe |
S62 |
6 | BAA02g46320 | A02 | 37690084 | G | A | upstream_gene_variant | MODIFIER | c.-2195C>T| |
S203 |
7 | BAA02g46320 | A02 | 37691010 | C | A | upstream_gene_variant | MODIFIER | c.-3121G>T| |
S118 |
8 | BAA02g46320 | A02 | 37692096 | C | T | upstream_gene_variant | MODIFIER | c.-4207G>A| |
S277 |