"Invitae"[submitter] AND "FBXW7"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2170337	NM_001349798.2(FBXW7):c.2116A>G (p.Met706Val)	FBXW7 (M588V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2704950	NM_001349798.2(FBXW7):c.1866G>A (p.Lys622=)	FBXW7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2848962	NM_001349798.2(FBXW7):c.1855+12_1855+15del	FBXW7	Deletion (intron variant)	not provided	GLikely benign
Select item 2713418	NM_001349798.2(FBXW7):c.1540G>A (p.Val514Ile)	FBXW7 (V396I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2710224	NM_001349798.2(FBXW7):c.1236+16del	FBXW7	Deletion (intron variant)	not provided	GLikely benign
Select item 2703871	NM_001349798.2(FBXW7):c.1120A>G (p.Lys374Glu)	FBXW7 (K294E +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2095485	NM_001349798.2(FBXW7):c.1031C>G (p.Pro344Arg)	FBXW7 (P264R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2708415	NM_001349798.2(FBXW7):c.967G>A (p.Glu323Lys)	FBXW7 (E205K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2712005	NM_001349798.2(FBXW7):c.726+19G>C	FBXW7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2702155	NM_001349798.2(FBXW7):c.726+2_726+5dup	FBXW7	Duplication (splice donor variant)	not provided	GUncertain significance
Select item 2896320	NM_001349798.2(FBXW7):c.536G>A (p.Arg179His)	FBXW7 (R179H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 134382	NM_001349798.2(FBXW7):c.397A>G (p.Arg133Gly)	FBXW7 (R133G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2879477	NM_001349798.2(FBXW7):c.378T>A (p.Asp126Glu)	FBXW7 (D126E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2179801	NM_001349798.2(FBXW7):c.227A>T (p.Gln76Leu)	FBXW7 (Q76L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 134381	NM_001349798.2(FBXW7):c.45_46insCCT (p.Thr15_Gly16insPro)	FBXW7	Insertion (inframe_insertion)	FBXW7-related condition +1 more	GBenign/Likely benign
Select item 2892307	NM_001349798.2(FBXW7):c.45T>C (p.Thr15=)	FBXW7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign