Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g10800 | A03 | 4458158 | C | T | synonymous_variant | LOW | c.2502G>A|p.Gly834Gly |
S164 |
2 | BAA03g10800 | A03 | 4458758 | C | T | missense_variant | MODERATE | c.2194G>A|p.Glu732Lys |
S265 |
3 | BAA03g10800 | A03 | 4459592 | C | T | missense_variant | MODERATE | c.1615G>A|p.Val539Met |
S259 |
4 | BAA03g10800 | A03 | 4460257 | C | T | missense_variant | MODERATE | c.1318G>A|p.Val440Ile |
S210 |
5 | BAA03g10800 | A03 | 4461100 | C | T | missense_variant | MODERATE | c.1037G>A|p.Arg346Lys |
S107 |
6 | BAA03g10800 | A03 | 4462426 | G | A | synonymous_variant | LOW | c.360C>T|p.Asn120Asn |
S262 |
7 | BAA03g10800 | A03 | 4462805 | G | A | missense_variant | MODERATE | c.179C>T|p.Ser60Leu |
S57 |
8 | BAA03g10800 | A03 | 4465698 | G | A | upstream_gene_variant | MODIFIER | c.-2429C>T| |
S116 |
9 | BAA03g10800 | A03 | 4466026 | G | A | upstream_gene_variant | MODIFIER | c.-2757C>T| |
S246 |
10 | BAA03g10800 | A03 | 4466184 | C | T | upstream_gene_variant | MODIFIER | c.-2915G>A| |
S38 |