"FOXF2-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055662	NM_001452.2(FOXF2):c.97GCC[10] (p.Ala41_Pro42insAla)	FOXF2	Microsatellite (inframe insertion)	FOXF2-related disorder	GBenign
Select item 3055285	NM_001452.2(FOXF2):c.97GCC[8] (p.Ala41del)	FOXF2 (A41del)	Microsatellite (inframe deletion)	FOXF2-related disorder	GBenign
Select item 3047212	NM_001452.2(FOXF2):c.97GCC[5] (p.Ala38_Ala41del)	FOXF2	Microsatellite (inframe deletion)	FOXF2-related disorder	GLikely benign
Select item 3041547	NM_001452.2(FOXF2):c.97GCC[6] (p.Ala39_Ala41del)	FOXF2	Microsatellite (inframe deletion)	FOXF2-related disorder	GLikely benign
Select item 3045896	NM_001452.2(FOXF2):c.121G>T (p.Ala41Ser)	FOXF2 (A41S)	Single nucleotide variant (missense variant)	FOXF2-related disorder	GLikely benign
Select item 3031764	NM_001452.2(FOXF2):c.126G>A (p.Pro42=)	FOXF2	Single nucleotide variant (synonymous variant)	FOXF2-related disorder	GLikely benign
Select item 3055942	NM_001452.2(FOXF2):c.203C>T (p.Ala68Val)	FOXF2 (A68V)	Single nucleotide variant (missense variant)	FOXF2-related disorder	GLikely benign
Select item 3044929	NM_001452.2(FOXF2):c.240C>T (p.Gly80=)	FOXF2	Single nucleotide variant (synonymous variant)	FOXF2-related disorder	GLikely benign
Select item 3031696	NM_001452.2(FOXF2):c.375G>A (p.Glu125=)	FOXF2, MIR6720	Single nucleotide variant (non-coding transcript variant +1 more)	FOXF2-related disorder	GLikely benign
Select item 3036232	NM_001452.2(FOXF2):c.447C>T (p.Arg149=)	FOXF2, MIR6720	Single nucleotide variant (non-coding transcript variant +1 more)	FOXF2-related disorder	GLikely benign
Select item 3057858	NM_001452.2(FOXF2):c.663G>A (p.Leu221=)	FOXF2	Single nucleotide variant (synonymous variant)	FOXF2-related disorder	GLikely benign
Select item 3056857	NM_001452.2(FOXF2):c.796CAC[6] (p.His272del)	FOXF2 (H272del)	Microsatellite (inframe deletion)	FOXF2-related disorder	GLikely benign
Select item 3033923	NM_001452.2(FOXF2):c.812A>G (p.His271Arg)	FOXF2 (H271R)	Single nucleotide variant (missense variant)	FOXF2-related disorder	GLikely benign
Select item 3039669	NM_001452.2(FOXF2):c.1323C>A (p.Pro441=)	FOXF2	Single nucleotide variant (synonymous variant)	FOXF2-related disorder	GBenign
Select item 3050000	NM_001452.2(FOXF2):c.*2C>A	FOXF2	Single nucleotide variant (3 prime UTR variant)	FOXF2-related disorder	GBenign