"Ambry Genetics"[submitter] AND "CYP26C1"[gene] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2338459	NM_183374.3(CYP26C1):c.121C>T (p.Arg41Trp)	CYP26C1 (R41W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079432	NM_183374.3(CYP26C1):c.173T>A (p.Phe58Tyr)	CYP26C1 (F58Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615557	NM_183374.3(CYP26C1):c.206G>A (p.Gly69Asp)	CYP26C1 (G69D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270523	NM_183374.3(CYP26C1):c.277G>C (p.Val93Leu)	CYP26C1 (V93L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515104	NM_183374.3(CYP26C1):c.316C>G (p.Leu106Val)	CYP26C1 (L106V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617062	NM_183374.3(CYP26C1):c.328C>T (p.His110Tyr)	CYP26C1 (H110Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270522	NM_183374.3(CYP26C1):c.355C>G (p.Gln119Glu)	CYP26C1 (Q119E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325518	NM_183374.3(CYP26C1):c.364C>T (p.His122Tyr)	CYP26C1 (H122Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242780	NM_183374.3(CYP26C1):c.395G>T (p.Gly132Val)	CYP26C1 (G132V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219206	NM_183374.3(CYP26C1):c.407A>G (p.Glu136Gly)	CYP26C1 (E136G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079433	NM_183374.3(CYP26C1):c.419G>T (p.Arg140Leu)	CYP26C1 (R140L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257834	NM_183374.3(CYP26C1):c.464A>C (p.Glu155Ala)	CYP26C1, LOC130004370 (E155A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079434	NM_183374.3(CYP26C1):c.529G>A (p.Gly177Arg)	CYP26C1, LOC130004371 (G177R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2402269	NM_183374.3(CYP26C1):c.547G>C (p.Asp183His)	CYP26C1, LOC130004371 (D183H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079435	NM_183374.3(CYP26C1):c.550G>A (p.Ala184Thr)	CYP26C1, LOC130004371 (A184T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361457	NM_183374.3(CYP26C1):c.572G>T (p.Arg191Leu)	CYP26C1, LOC130004371 (R191L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242581	NM_183374.3(CYP26C1):c.632C>G (p.Ala211Gly)	CYP26C1, LOC130004371 (A211G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375831	NM_183374.3(CYP26C1):c.685C>G (p.Pro229Ala)	CYP26C1, LOC130004371 (P229A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318380	NM_183374.3(CYP26C1):c.772G>T (p.Asp258Tyr)	CYP26C1 (D258Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407843	NM_183374.3(CYP26C1):c.916A>G (p.Thr306Ala)	CYP26C1 (T306A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079426	NM_183374.3(CYP26C1):c.1027G>T (p.Gly343Trp)	CYP26C1 (G343W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270614	NM_183374.3(CYP26C1):c.1028G>A (p.Gly343Glu)	CYP26C1 (G343E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364136	NM_183374.3(CYP26C1):c.1036G>A (p.Glu346Lys)	CYP26C1 (E346K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309342	NM_183374.3(CYP26C1):c.1042C>T (p.Pro348Ser)	CYP26C1 (P348S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270525	NM_183374.3(CYP26C1):c.1099C>T (p.Arg367Cys)	CYP26C1 (R367C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079428	NM_183374.3(CYP26C1):c.1126G>C (p.Val376Leu)	CYP26C1 (V376L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526461	NM_183374.3(CYP26C1):c.1192G>A (p.Gly398Ser)	CYP26C1 (G398S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544281	NM_183374.3(CYP26C1):c.1215G>C (p.Trp405Cys)	CYP26C1 (W405C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302127	NM_183374.3(CYP26C1):c.1259T>C (p.Val420Ala)	CYP26C1 (V420A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348150	NM_183374.3(CYP26C1):c.1273C>T (p.Pro425Ser)	CYP26C1 (P425S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2471516	NM_183374.3(CYP26C1):c.1303G>T (p.Ala435Ser)	CYP26C1 (A435S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547107	NM_183374.3(CYP26C1):c.1313A>G (p.Glu438Gly)	CYP26C1 (E438G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548322	NM_183374.3(CYP26C1):c.1367C>A (p.Ala456Glu)	CYP26C1 (A456E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243638	NM_183374.3(CYP26C1):c.1378C>T (p.Leu460Phe)	CYP26C1 (L460F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079430	NM_183374.3(CYP26C1):c.1394C>T (p.Ala465Val)	CYP26C1 (A465V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370749	NM_183374.3(CYP26C1):c.1400C>A (p.Ala467Asp)	CYP26C1 (A467D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491922	NM_183374.3(CYP26C1):c.1426C>A (p.Leu476Ile)	CYP26C1 (L476I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079431	NM_183374.3(CYP26C1):c.1436C>G (p.Thr479Ser)	CYP26C1 (T479S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222559	NM_183374.3(CYP26C1):c.1468C>A (p.Pro490Thr)	CYP26C1 (P490T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216996	NM_183374.3(CYP26C1):c.1471G>A (p.Ala491Thr)	CYP26C1 (A491T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209572	NM_183374.3(CYP26C1):c.1507G>A (p.Gly503Arg)	CYP26C1 (G503R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 41