"PreventionGenetics, part of Exact Sciences"[submitter] AND "CYP4F2"[g - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3031223	NM_001082.5(CYP4F2):c.*8A>G	CYP4F2	Single nucleotide variant (3 prime UTR variant)	CYP4F2-related disorder	GLikely benign
Select item 3056325	NM_001082.5(CYP4F2):c.1555C>A (p.Leu519Met)	CYP4F2 (L519M)	Single nucleotide variant (missense variant)	CYP4F2-related disorder	GLikely benign
Select item 3047382	NM_001082.5(CYP4F2):c.1543C>A (p.Arg515=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GLikely benign
Select item 3054703	NM_001082.5(CYP4F2):c.1470C>T (p.Arg490=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GLikely benign
Select item 3031316	NM_001082.5(CYP4F2):c.1443C>T (p.Val481=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GLikely benign
Select item 3059292	NM_001082.5(CYP4F2):c.1414A>G (p.Thr472Ala)	CYP4F2 (T472A)	Single nucleotide variant (missense variant)	CYP4F2-related disorder	GLikely benign
Select item 3038214	NM_001082.5(CYP4F2):c.1398-4C>G	CYP4F2	Single nucleotide variant (intron variant)	CYP4F2-related disorder	GBenign
Select item 225969	NM_001082.5(CYP4F2):c.1297G>A (p.Val433Met)	CYP4F2 (V433M)	Single nucleotide variant (missense variant)	warfarin response - Dosage +1 more	Gdrug response
Select item 3049482	NM_001082.5(CYP4F2):c.1242C>T (p.Ile414=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GLikely benign
Select item 771214	NM_001082.5(CYP4F2):c.1115+10G>A	CYP4F2	Single nucleotide variant (intron variant)	CYP4F2-related disorder +1 more	GBenign
Select item 3052749	NM_001082.5(CYP4F2):c.1092C>T (p.Asp364=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GLikely benign
Select item 3056285	NM_001082.5(CYP4F2):c.1029C>T (p.His343=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GBenign
Select item 3033266	NM_001082.5(CYP4F2):c.919-9T>G	CYP4F2	Single nucleotide variant (intron variant)	CYP4F2-related disorder	GLikely benign
Select item 3048385	NM_001082.5(CYP4F2):c.792C>T (p.His264=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GLikely benign
Select item 3055377	NM_001082.5(CYP4F2):c.554G>T (p.Gly185Val)	CYP4F2 (G185V)	Single nucleotide variant (missense variant)	CYP4F2-related disorder	GBenign
Select item 3040636	NM_001082.5(CYP4F2):c.343+6A>G	CYP4F2	Single nucleotide variant (intron variant)	CYP4F2-related disorder	GLikely benign
Select item 3055271	NM_001082.5(CYP4F2):c.336C>T (p.Asn112=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GBenign
Select item 3055346	NM_001082.5(CYP4F2):c.279A>C (p.Gly93=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GBenign
Select item 3060160	NM_001082.5(CYP4F2):c.246C>T (p.Ala82=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GBenign
Select item 3044148	NM_001082.5(CYP4F2):c.240G>T (p.Leu80=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GLikely benign
Select item 3060298	NM_001082.5(CYP4F2):c.165A>G (p.Pro55=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GBenign
Select item 3044144	NM_001082.5(CYP4F2):c.99T>C (p.His33=)	CYP4F2	Single nucleotide variant (synonymous variant)	CYP4F2-related disorder	GLikely benign
Select item 3052405	NM_001082.5(CYP4F2):c.46G>C (p.Ala16Pro)	CYP4F2 (A16P)	Single nucleotide variant (missense variant)	CYP4F2-related disorder	GBenign

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Items: 23