"Ambry Genetics"[submitter] AND "FBXO5"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2603047	NM_012177.5(FBXO5):c.1334G>A (p.Arg445Gln)	FBXO5 (R399Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3093789	NM_012177.5(FBXO5):c.1294G>C (p.Gly432Arg)	FBXO5 (G386R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219404	NM_012177.5(FBXO5):c.1279G>A (p.Ala427Thr)	FBXO5 (A381T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336939	NM_012177.5(FBXO5):c.1247C>T (p.Thr416Ile)	FBXO5 (T370I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595635	NM_012177.5(FBXO5):c.1127A>G (p.Lys376Arg)	FBXO5 (K330R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545792	NM_012177.5(FBXO5):c.1073G>A (p.Arg358Gln)	FBXO5 (R358Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278206	NM_012177.5(FBXO5):c.931C>T (p.Pro311Ser)	FBXO5 (P311S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093798	NM_012177.5(FBXO5):c.904G>C (p.Val302Leu)	FBXO5 (V302L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093797	NM_012177.5(FBXO5):c.845A>G (p.Lys282Arg)	FBXO5 (K282R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403239	NM_012177.5(FBXO5):c.808G>T (p.Asp270Tyr)	FBXO5 (D224Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330226	NM_012177.5(FBXO5):c.770A>G (p.His257Arg)	FBXO5 (H257R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528626	NM_012177.5(FBXO5):c.632G>A (p.Arg211Gln)	FBXO5 (R165Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318435	NM_012177.5(FBXO5):c.605G>C (p.Cys202Ser)	FBXO5 (C202S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093794	NM_012177.5(FBXO5):c.559C>T (p.Pro187Ser)	FBXO5 (P187S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093793	NM_012177.5(FBXO5):c.499G>A (p.Glu167Lys)	FBXO5 (E121K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297589	NM_012177.5(FBXO5):c.412A>G (p.Thr138Ala)	FBXO5 (T138A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278208	NM_012177.5(FBXO5):c.347A>G (p.His116Arg)	FBXO5 (H116R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357301	NM_012177.5(FBXO5):c.296C>T (p.Pro99Leu)	FBXO5 (P53L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093792	NM_012177.5(FBXO5):c.164A>G (p.His55Arg)	FBXO5 (H55R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093790	NM_012177.5(FBXO5):c.131C>T (p.Ser44Phe)	FBXO5 (S44F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3093796	NM_012177.5(FBXO5):c.70G>T (p.Val24Leu)	FBXO5 (V24L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3093795	NM_012177.5(FBXO5):c.68C>T (p.Ala23Val)	FBXO5 (A23V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403649	NM_012177.5(FBXO5):c.64A>G (p.Ser22Gly)	FBXO5 (S22G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480710	NM_012177.5(FBXO5):c.59G>A (p.Ser20Asn)	FBXO5 (S20N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093791	NM_012177.5(FBXO5):c.14C>T (p.Pro5Leu)	FBXO5 (P5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 25