Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15870 | A10 | 16026149 | C | T | missense_variant | MODERATE | c.1166G>A|p.Gly389Glu |
S232 |
2 | BAA10g15870 | A10 | 16026567 | G | A | missense_variant | MODERATE | c.748C>T|p.Leu250Phe |
S292 |
3 | BAA10g15870 | A10 | 16026951 | G | A | synonymous_variant | LOW | c.364C>T|p.Leu122Leu |
S35 |
4 | BAA10g15870 | A10 | 16027833 | C | T | missense_variant | MODERATE | c.175G>A|p.Glu59Lys |
S135 |
5 | BAA10g15870 | A10 | 16032904 | G | A | upstream_gene_variant | MODIFIER | c.-4897C>T| |
S234 |