Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.42127608C>TCA10264686CYP2D6c.810G>A (n.810G>A)
c.1012G>A (p.Val338Met)
c.859G>A (p.Val287Met)
c.630G>A (n.630G>A)
c.1003G>A (p.Val335Met)
n.1736G>A
c.868G>A (p.Val290Met)
c.870G>A (p.Thr290=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.42127608C>ACA411771903CYP2D6c.810G>T (n.810G>T)
c.1012G>T (p.Val338Leu)
c.859G>T (p.Val287Leu)
c.630G>T (n.630G>T)
c.1003G>T (p.Val335Leu)
n.1736G>T
c.868G>T (p.Val290Leu)
c.870G>T (p.Thr290=)
dbSNP
22g.42127608C>GCA411771904CYP2D6c.810G>C (n.810G>C)
c.1012G>C (p.Val338Leu)
c.859G>C (p.Val287Leu)
c.630G>C (n.630G>C)
c.1003G>C (p.Val335Leu)
n.1736G>C
c.868G>C (p.Val290Leu)
c.870G>C (p.Thr290=)
dbSNP gnomAD v4
22g.42127608C=CA2406578554CYP2D6c.810G= (n.810G=)
c.1012G= (p.Val338=)
c.859G= (p.Val287=)
c.630G= (n.630G=)
c.1003G= (p.Val335=)
n.1736G=
c.868G= (p.Val290=)
c.870G= (p.Thr290=)
dbSNP dbSNP

Number of alleles fetched