Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.855978G>T | CA281046 | ELANE | c.618G>T (p.Leu206Phe) | ClinVar dbSNP |
19 | g.855978G>C | CA402918918 | ELANE | c.618G>C (p.Leu206Phe) | ClinVar dbSNP |
19 | g.855978G= | CA2317361608 | ELANE | c.618G= (p.Leu206=) | dbSNP |
19 | g.855978G>A | CA504686387 | ELANE | c.618G>A (p.Leu206=) | ClinVar dbSNP |