Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.8112168A>G | CA287526914 | ALOXE3 | c.709T>C (p.Leu237=) c.1105T>C (p.Leu369=) c.1177T>C (p.Leu393=) n.982T>C c.706T>C (p.Leu236=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.8112168A>T | CA116202 | ALOXE3 | c.709T>A (p.Leu237Met) c.1105T>A (p.Leu369Met) c.1177T>A (p.Leu393Met) n.982T>A c.706T>A (p.Leu236Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |