"Ambry Genetics"[submitter] AND "FCER2"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2371351	NM_001220500.2(FCER2):c.916C>T (p.Pro306Ser)	FCER2 (P306S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316738	NM_001220500.2(FCER2):c.824G>A (p.Arg275His)	FCER2 (R275H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532312	NM_001220500.2(FCER2):c.812C>A (p.Ala271Asp)	FCER2 (A270D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518102	NM_001220500.2(FCER2):c.800G>C (p.Arg267Pro)	FCER2 (R267P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524275	NM_001220500.2(FCER2):c.788G>A (p.Arg263Gln)	FCER2 (R262Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3093925	NM_001220500.2(FCER2):c.736G>T (p.Ala246Ser)	FCER2 (A246S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361041	NM_001220500.2(FCER2):c.656C>T (p.Ser219Phe)	FCER2 (S218F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365835	NM_001220500.2(FCER2):c.616G>A (p.Glu206Lys)	FCER2 (E205K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242007	NM_001220500.2(FCER2):c.586G>A (p.Gly196Arg)	FCER2 (G196R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243089	NM_001220500.2(FCER2):c.520T>A (p.Cys174Ser)	FCER2 (C173S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270316	NM_001220500.2(FCER2):c.458A>C (p.Gln153Pro)	FCER2 (Q152P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409891	NM_001220500.2(FCER2):c.424C>T (p.Arg142Trp)	FCER2 (R141W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245957	NM_001220500.2(FCER2):c.343G>A (p.Gly115Arg)	FCER2 (G114R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2514848	NM_001220500.2(FCER2):c.305T>C (p.Leu102Ser)	FCER2 (L101S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268240	NM_001220500.2(FCER2):c.262A>G (p.Ile88Val)	FCER2 (I87V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093923	NM_001220500.2(FCER2):c.208A>G (p.Asn70Asp)	FCER2 (N70D +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2237688	NM_001220500.2(FCER2):c.146C>T (p.Thr49Ile)	FCER2 (T48I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211419	NM_001220500.2(FCER2):c.110G>A (p.Gly37Glu)	FCER2 (G37E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093927	NM_001220500.2(FCER2):c.97G>A (p.Ala33Thr)	FCER2 (A33T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271486	NM_001220500.2(FCER2):c.92C>T (p.Thr31Ile)	FCER2 (T30I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093926	NM_001220500.2(FCER2):c.83G>A (p.Gly28Glu)	FCER2 (G27E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203890	NM_001220500.2(FCER2):c.59G>A (p.Arg20His)	FCER2 (R19H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509578	NM_001220500.2(FCER2):c.28G>A (p.Glu10Lys)	FCER2 (E10K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 23