"Ambry Genetics"[submitter] AND "CYP2D6"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2279487	NM_000106.6(CYP2D6):c.1471G>A (p.Glu491Lys)	CYP2D6 (E440K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362239	NM_000106.6(CYP2D6):c.1386G>C (p.Gln462His)	CYP2D6 (Q411H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593898	NM_000106.6(CYP2D6):c.1324G>A (p.Ala442Thr)	CYP2D6 (A391T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079534	NM_000106.6(CYP2D6):c.1241G>A (p.Arg414His)	CYP2D6 (R414H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519209	NM_000106.6(CYP2D6):c.1144A>G (p.Ile382Val)	CYP2D6 (I331V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325972	NM_000106.6(CYP2D6):c.1112C>T (p.Pro371Leu)	CYP2D6 (P371L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516274	NM_000106.6(CYP2D6):c.1075G>A (p.Val359Met)	CYP2D6 (V359M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287538	NM_000106.6(CYP2D6):c.1055A>T (p.His352Leu)	CYP2D6 (H352L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397540	NM_000106.6(CYP2D6):c.910T>C (p.Ser304Pro)	CYP2D6 (S304P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079538	NM_000106.6(CYP2D6):c.853A>T (p.Asn285Tyr)	CYP2D6 (N234Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486829	NM_000106.6(CYP2D6):c.802C>A (p.Pro268Thr)	CYP2D6 (P217T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460658	NM_000106.6(CYP2D6):c.688C>T (p.Leu230Phe)	CYP2D6 (L230F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546859	NM_000106.6(CYP2D6):c.679G>C (p.Val227Leu)	CYP2D6 (V176L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257333	NM_000106.6(CYP2D6):c.667G>T (p.Val223Leu)	CYP2D6 (V172L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296692	NM_000106.6(CYP2D6):c.640A>C (p.Lys214Gln)	CYP2D6 (K214Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079537	NM_000106.6(CYP2D6):c.598C>G (p.Pro200Ala)	CYP2D6 (P149A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485653	NM_000106.6(CYP2D6):c.598C>T (p.Pro200Ser)	CYP2D6 (P200S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349106	NM_000106.6(CYP2D6):c.502T>G (p.Ser168Ala)	CYP2D6 (S168A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2457990	NM_000106.6(CYP2D6):c.468G>C (p.Glu156Asp)	CYP2D6 (E156D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378169	NM_000106.6(CYP2D6):c.445C>A (p.Leu149Met)	CYP2D6 (L149M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341282	NM_000106.6(CYP2D6):c.376C>A (p.Pro126Thr)	CYP2D6 (P126T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079536	NM_000106.6(CYP2D6):c.314C>T (p.Pro105Leu)	CYP2D6 (P105L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079535	NM_000106.6(CYP2D6):c.305C>T (p.Pro102Leu)	CYP2D6 (P102L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467185	NM_000106.6(CYP2D6):c.245A>C (p.Asn82Thr)	CYP2D6 (N82T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 829634	NM_000106.6(CYP2D6):c.145G>A (p.Val49Met)	CYP2D6 (V49M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079539	NM_000106.6(CYP2D6):c.94C>T (p.Arg32Cys)	CYP2D6 (R32C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342095	NM_000106.6(CYP2D6):c.76C>T (p.Arg26Cys)	CYP2D6 (R26C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27