Related gene-specific medical variations for Gene (Select 26259) - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2609746	NM_153348.3(FBXW8):c.1002G>C (p.Gln334His)	FBXW8, LOC100506551 (Q268H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2608017	NM_153348.3(FBXW8):c.1441G>A (p.Val481Met)	FBXW8, LOC126861650 (V481M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2509673	NM_153348.3(FBXW8):c.299A>G (p.Asp100Gly)	FBXW8, LOC130008877 (D100G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2467559	NM_153348.3(FBXW8):c.928G>C (p.Asp310His)	FBXW8, LOC100506551 (D244H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2456897	NM_153348.3(FBXW8):c.1508G>A (p.Arg503Gln)	FBXW8, LOC126861650 (R503Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2396828	NM_153348.3(FBXW8):c.967G>A (p.Val323Met)	LOC100506551, FBXW8 (V323M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2361998	NM_153348.3(FBXW8):c.1465G>A (p.Val489Ile)	FBXW8, LOC126861650 (V423I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2323691	NM_153348.3(FBXW8):c.854A>G (p.Asp285Gly)	LOC100506551, FBXW8 (D285G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2268239	NM_153348.3(FBXW8):c.313G>C (p.Asp105His)	FBXW8, LOC130008877 (D105H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2232864	NM_153348.3(FBXW8):c.239C>G (p.Ala80Gly)	FBXW8, LOC130008877 (A80G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2227809	NM_153348.3(FBXW8):c.263C>G (p.Ala88Gly)	FBXW8, LOC130008877 (A88G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2217823	NM_153348.3(FBXW8):c.983A>G (p.Asn328Ser)	FBXW8, LOC100506551 (N262S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2210742	NM_153348.3(FBXW8):c.931G>A (p.Asp311Asn)	FBXW8, LOC100506551 (D245N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 790128	NM_153348.3(FBXW8):c.1030C>T (p.Leu344=)	FBXW8, LOC100506551	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 721845	NM_153348.3(FBXW8):c.222C>T (p.Ala74=)	FBXW8, LOC130008877	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign