"Ambry Genetics"[submitter] AND "FBXL22"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3093535	NM_001367807.1(FBXL22):c.93C>G (p.Ser31Arg)	FBXL22, USP3-AS1 (S31R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093528	NM_001367807.1(FBXL22):c.121G>A (p.Asp41Asn)	FBXL22, USP3-AS1 (D41N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482271	NM_001367807.1(FBXL22):c.163C>A (p.Arg55Ser)	FBXL22, USP3-AS1 (R55S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301284	NM_001367807.1(FBXL22):c.167C>T (p.Ser56Phe)	FBXL22, USP3-AS1 (S56F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551787	NM_001367807.1(FBXL22):c.206C>G (p.Pro69Arg)	FBXL22, USP3-AS1 (P69R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204106	NM_001367807.1(FBXL22):c.215G>A (p.Arg72His)	FBXL22, USP3-AS1 (R72H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268565	NM_001367807.1(FBXL22):c.251A>G (p.Gln84Arg)	FBXL22, USP3-AS1 (Q84R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093529	NM_001367807.1(FBXL22):c.263T>C (p.Ile88Thr)	FBXL22, USP3-AS1 (I88T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093530	NM_001367807.1(FBXL22):c.274C>G (p.Leu92Val)	FBXL22, USP3-AS1 (L92V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350157	NM_001367807.1(FBXL22):c.281G>A (p.Ser94Asn)	FBXL22, USP3-AS1 (S94N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229638	NM_001367807.1(FBXL22):c.313G>C (p.Glu105Gln)	FBXL22, USP3-AS1 (E105Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093531	NM_203373.3(FBXL22):c.445G>A (p.Gly149Arg)	FBXL22 (G149R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2396773	NM_203373.3(FBXL22):c.479G>T (p.Arg160Leu)	FBXL22 (R160L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3093532	NM_203373.3(FBXL22):c.494G>C (p.Gly165Ala)	FBXL22 (G165A)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2308901	NM_203373.3(FBXL22):c.496G>A (p.Ala166Thr)	FBXL22 (A166T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3093533	NM_203373.3(FBXL22):c.508G>C (p.Ala170Pro)	FBXL22 (A170P)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2263076	NM_203373.3(FBXL22):c.562G>C (p.Ala188Pro)	FBXL22 (A188P)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2294659	NM_203373.3(FBXL22):c.614C>T (p.Ser205Leu)	FBXL22 (S205L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2332144	NM_203373.3(FBXL22):c.652A>G (p.Arg218Gly)	FBXL22 (R218G)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3093534	NM_203373.3(FBXL22):c.676C>T (p.Pro226Ser)	FBXL22 (P226S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2624028	NM_203373.3(FBXL22):c.694A>G (p.Thr232Ala)	FBXL22 (T232A)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 21