Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g56080 | A09 | 55914175 | C | T | missense_variant | MODERATE | c.1096G>A|p.Gly366Ser |
S61 |
2 | BAA09g56080 | A09 | 55914696 | C | T | synonymous_variant | LOW | c.702G>A|p.Leu234Leu |
S204 |
3 | BAA09g56080 | A09 | 55914765 | C | T | synonymous_variant | LOW | c.633G>A|p.Lys211Lys |
S260 |
4 | BAA09g56080 | A09 | 55914815 | G | A | missense_variant | MODERATE | c.583C>T|p.Pro195Ser |
S2 |
5 | BAA09g56080 | A09 | 55914979 | G | A | missense_variant | MODERATE | c.419C>T|p.Pro140Leu |
S88 |
6 | BAA09g56080 | A09 | 55915139 | C | T | missense_variant | MODERATE | c.259G>A|p.Asp87Asn |
S168 |
7 | BAA09g56080 | A09 | 55915242 | G | A | synonymous_variant | LOW | c.156C>T|p.Leu52Leu |
S202 |
8 | BAA09g56080 | A09 | 55917122 | G | A | upstream_gene_variant | MODIFIER | c.-1725C>T| |
S116 |
9 | BAA09g56080 | A09 | 55918389 | G | A | upstream_gene_variant | MODIFIER | c.-2992C>T| |
S172 S217 |
10 | BAA09g56080 | A09 | 55918888 | G | A | upstream_gene_variant | MODIFIER | c.-3491C>T| |
S47 |