Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.42127928G>TCA411772679CYP2D6c.697C>A (p.Leu233Met)
c.899C>A (p.Ala300Asp)
c.746C>A (p.Ala249Asp)
c.517C>A (p.Leu173Met)
c.833C>A (p.Ala278Asp)
n.1623C>A
c.755C>A (p.Ala252Asp)
c.843+246C>A (n.843+246C>A)
dbSNP gnomAD v2 gnomAD v4
22g.42127928G>ACA411772676CYP2D6c.697C>T (p.Leu233=)
c.899C>T (p.Ala300Val)
c.746C>T (p.Ala249Val)
c.517C>T (p.Leu173=)
c.833C>T (p.Ala278Val)
n.1623C>T
c.755C>T (p.Ala252Val)
c.843+246C>T (n.843+246C>T)
dbSNP
22g.42127928G>CCA324666463CYP2D6c.697C>G (p.Leu233Val)
c.899C>G (p.Ala300Gly)
c.746C>G (p.Ala249Gly)
c.517C>G (p.Leu173Val)
c.833C>G (p.Ala278Gly)
n.1623C>G
c.755C>G (p.Ala252Gly)
c.843+246C>G (n.843+246C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched