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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP2D6
(S486T +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign; other
CYP2D6
(V338M +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign; other
CYP2D6
Single nucleotide variant
(intron variant)
not provided
+2 more
GLikely benign; drug response; other
CYP2D6
(H324P +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign; other
CYP2D6
Single nucleotide variant
not provided
Gother
CYP2D6
(K281del +1 more)
Deletion
(inframe_deletion)
not provided
GLikely benign; other
CYP2D6
(R259fs +1 more)
Deletion
(frameshift variant)
not provided
GLikely benign; other
CYP2D6
Single nucleotide variant
(splice acceptor variant)
not specified
+3 more
GLikely benign; drug response; other
CYP2D6
(G169R)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign; other
CYP2D6
(G169*)
Single nucleotide variant
(nonsense +1 more)
not provided
GLikely benign; other
CYP2D6
(W152fs)
Deletion
(frameshift variant +1 more)
not provided
+2 more
GBenign/Likely benign; drug response; other
CYP2D6
(T107I)
Single nucleotide variant
(missense variant)
not provided
GLikely benign; other
CYP2D6
(G42R)
Single nucleotide variant
(missense variant)
not provided
GLikely benign; other
CYP2D6
(P34S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GLikely benign; drug response; other
CYP2D6, LOC110740340
Single nucleotide variant
(genic upstream transcript variant)
not provided
Gother
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