CYP26A1[gene] and "single gene"[properties] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2271742	NM_000783.4(CYP26A1):c.86A>G (p.Asp29Gly)	CYP26A1 (D29G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616570	NM_000783.4(CYP26A1):c.140G>A (p.Gly47Glu)	CYP26A1 (G47E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079407	NM_000783.4(CYP26A1):c.143C>T (p.Thr48Ile)	CYP26A1 (T48I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079408	NM_000783.4(CYP26A1):c.305T>A (p.Leu102His)	CYP26A1 (L102H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481978	NM_000783.4(CYP26A1):c.350G>T (p.Arg117Leu)	CYP26A1 (R48L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079409	NM_000783.4(CYP26A1):c.424C>T (p.Arg142Trp)	CYP26A1 (R142W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775288	NM_000783.4(CYP26A1):c.432C>T (p.Phe144=)	CYP26A1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2221999	NM_000783.4(CYP26A1):c.436C>T (p.Arg146Cys)	CYP26A1 (R146C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 778469	NM_000783.4(CYP26A1):c.447C>G (p.Leu149=)	CYP26A1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2373958	NM_000783.4(CYP26A1):c.472G>A (p.Glu158Lys)	CYP26A1 (E89K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079410	NM_000783.4(CYP26A1):c.488G>A (p.Ser163Asn)	CYP26A1 (S163N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475816	NM_000783.4(CYP26A1):c.545A>G (p.Lys182Arg)	CYP26A1 (K182R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079412	NM_000783.4(CYP26A1):c.731A>G (p.His244Arg)	CYP26A1 (H175R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274646	NM_000783.4(CYP26A1):c.741C>G (p.Ile247Met)	CYP26A1 (I247M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079413	NM_000783.4(CYP26A1):c.742G>C (p.Glu248Gln)	CYP26A1 (E248Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079414	NM_000783.4(CYP26A1):c.790G>C (p.Gly264Arg)	CYP26A1 (G264R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256061	NM_000783.4(CYP26A1):c.795G>C (p.Gln265His)	CYP26A1 (Q196H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270775	NM_000783.4(CYP26A1):c.853C>G (p.Leu285Val)	CYP26A1 (L285V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640682	NM_000783.4(CYP26A1):c.865-8A>G	CYP26A1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 208185	NM_000783.4(CYP26A1):c.905A>G (p.His302Arg)	CYP26A1 (H302R +1 more)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 2457143	NM_000783.4(CYP26A1):c.914C>T (p.Thr305Met)	CYP26A1 (T236M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079415	NM_000783.4(CYP26A1):c.964G>A (p.Val322Ile)	CYP26A1 (V322I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351279	NM_000783.4(CYP26A1):c.1039A>G (p.Met347Val)	CYP26A1 (M278V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252035	NM_000783.4(CYP26A1):c.1057C>T (p.Leu353Phe)	CYP26A1 (L284F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333555	NM_000783.4(CYP26A1):c.1066A>G (p.Ile356Val)	CYP26A1 (I287V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328411	NM_000783.4(CYP26A1):c.1093C>G (p.Arg365Gly)	CYP26A1 (R296G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293151	NM_000783.4(CYP26A1):c.1154G>A (p.Gly385Glu)	CYP26A1 (G385E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547838	NM_000783.4(CYP26A1):c.1177A>C (p.Asn393His)	CYP26A1 (N393H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 785324	NM_000783.4(CYP26A1):c.1191T>C (p.Ser397=)	CYP26A1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3079406	NM_000783.4(CYP26A1):c.1330G>A (p.Gly444Ser)	CYP26A1 (G375S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401732	NM_000783.4(CYP26A1):c.1426A>C (p.Thr476Pro)	CYP26A1 (T407P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 522175	NM_057157.2:c.1184T>C	CYP26A1	Single nucleotide variant	Optic nerve hypoplasia	GUncertain significance

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Items: 32