Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10440 | A10 | 12167772 | C | T | missense_variant | MODERATE | c.382C>T|p.Arg128Trp |
S87 |
2 | BAA10g10440 | A10 | 12167820 | G | A | missense_variant | MODERATE | c.430G>A|p.Glu144Lys |
S192 |
3 | BAA10g10440 | A10 | 12171190 | C | T | downstream_gene_variant | MODIFIER | c.*3260C>T| |
S152 |