Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00150 | A08 | 107673 | G | A | missense_variant | MODERATE | c.1043C>T|p.Thr348Met |
S148 S210 |
2 | BAA08g00150 | A08 | 107857 | C | T | missense_variant | MODERATE | c.956G>A|p.Ser319Asn |
S177 |
3 | BAA08g00150 | A08 | 108702 | C | T | missense_variant | MODERATE | c.562G>A|p.Glu188Lys |
S172 S217 |
4 | BAA08g00150 | A08 | 109157 | C | T | missense_variant | MODERATE | c.299G>A|p.Gly100Glu |
S122 |
5 | BAA08g00150 | A08 | 113424 | G | A | upstream_gene_variant | MODIFIER | c.-3800C>T| |
S249 |
6 | BAA08g00150 | A08 | 113450 | C | T | upstream_gene_variant | MODIFIER | c.-3826G>A| |
S205 |