Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26770 | A10 | 21092643 | G | A | missense_variant | MODERATE | c.247G>A|p.Val83Met |
S65 |
2 | BAA10g26770 | A10 | 21096161 | G | A | missense_variant | MODERATE | c.2258G>A|p.Arg753Lys |
S125 |
3 | BAA10g26770 | A10 | 21096457 | G | A | missense_variant | MODERATE | c.2467G>A|p.Val823Met |
S278 |
4 | BAA10g26770 | A10 | 21098655 | C | T | downstream_gene_variant | MODIFIER | c.*2166C>T| |
S140 |
5 | BAA10g26770 | A10 | 21099145 | G | A | downstream_gene_variant | MODIFIER | c.*2656G>A| |
S57 |