FBXL5[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278060	NM_012161.4(FBXL5):c.2013T>A (p.Asp671Glu)	FBXL5 (D671E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278062	NM_012161.4(FBXL5):c.1841A>G (p.His614Arg)	FBXL5 (H597R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307569	NM_012161.4(FBXL5):c.1784A>T (p.Glu595Val)	FBXL5 (E595V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243852	NM_012161.4(FBXL5):c.1694A>C (p.Glu565Ala)	FBXL5 (E564A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 219315	NM_012161.4(FBXL5):c.1654del (p.Cys552fs)	FBXL5 (C551fs +2 more)	Deletion (frameshift variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 2510611	NM_012161.4(FBXL5):c.1598G>T (p.Cys533Phe)	FBXL5 (C533F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361936	NM_012161.4(FBXL5):c.1570G>A (p.Asp524Asn)	FBXL5 (D398N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527340	NM_012161.4(FBXL5):c.1402C>G (p.Pro468Ala)	FBXL5 (P468A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093543	NM_012161.4(FBXL5):c.1377A>G (p.Ile459Met)	FBXL5 (I333M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278064	NM_012161.4(FBXL5):c.1346A>G (p.Asp449Gly)	FBXL5 (D448G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2497701	NM_012161.4(FBXL5):c.1345G>A (p.Asp449Asn)	FBXL5 (D323N +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2280918	NM_012161.4(FBXL5):c.1291T>A (p.Trp431Arg)	FBXL5 (W430R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260234	NM_012161.4(FBXL5):c.970G>A (p.Val324Ile)	FBXL5 (V198I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327017	NM_012161.4(FBXL5):c.944G>A (p.Arg315His)	FBXL5 (R189H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590193	NM_012161.4(FBXL5):c.943C>T (p.Arg315Cys)	FBXL5 (R189C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246695	NM_012161.4(FBXL5):c.905A>G (p.Glu302Gly)	FBXL5 (E176G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278061	NM_012161.4(FBXL5):c.902C>T (p.Ala301Val)	FBXL5 (A300V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236886	NM_012161.4(FBXL5):c.823G>A (p.Val275Met)	FBXL5 (V149M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471311	NM_012161.4(FBXL5):c.803C>T (p.Thr268Ile)	FBXL5 (T142I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093546	NM_012161.4(FBXL5):c.707C>A (p.Ser236Tyr)	FBXL5 (S236Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2253172	NM_012161.4(FBXL5):c.680G>A (p.Arg227Gln)	FBXL5 (R101Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093545	NM_012161.4(FBXL5):c.658C>T (p.Leu220Phe)	FBXL5 (L220F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411981	NM_012161.4(FBXL5):c.646A>G (p.Ile216Val)	FBXL5 (I215V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093544	NM_012161.4(FBXL5):c.634G>A (p.Val212Ile)	FBXL5 (V211I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 395095	GRCh37/hg19 4p15.32(chr4:15613881-15659599)x3	FBXL5	Copy number gain	See cases	GBenign/Likely benign

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Items: 25