Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41006936G>TCA215137CYP2B6c.516G>T (p.Gln172His)
c.484+2490G>T (p.=)
c.-75-1G>T (p.=)
c.364+2490G>T (p.=)
c.256+2490G>T (p.=)
n.100G>T
n.418G>T
ClinVar dbSNP ExAC gnomAD
19g.41006936G>ACA9455242CYP2B6c.516G>A (p.Gln172=)
c.484+2490G>A (p.=)
c.-75-1G>A (p.=)
c.364+2490G>A (p.=)
c.256+2490G>A (p.=)
n.100G>A
n.418G>A
dbSNP ExAC gnomAD

Number of alleles fetched