"Ambry Genetics"[submitter] AND "FCN3"[gene] - ClinVar

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

Search results

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2357442	NM_003665.4(FCN3):c.883C>T (p.Arg295Trp)	FCN3 (R284W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525557	NM_003665.4(FCN3):c.854G>A (p.Arg285His)	FCN3 (R285H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094168	NM_003665.4(FCN3):c.797G>C (p.Arg266Pro)	FCN3 (R266P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617267	NM_003665.4(FCN3):c.779G>A (p.Arg260Gln)	FCN3 (R260Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2216401	NM_003665.4(FCN3):c.779G>C (p.Arg260Pro)	FCN3 (R249P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535533	NM_003665.4(FCN3):c.659G>C (p.Gly220Ala)	FCN3 (G220A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094167	NM_003665.4(FCN3):c.649G>C (p.Gly217Arg)	FCN3 (G217R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382556	NM_003665.4(FCN3):c.595C>T (p.Arg199Cys)	FCN3 (R188C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493261	NM_003665.4(FCN3):c.565A>G (p.Asn189Asp)	FCN3 (N189D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094166	NM_003665.4(FCN3):c.539G>A (p.Arg180Gln)	FCN3 (R180Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216517	NM_003665.4(FCN3):c.512T>C (p.Leu171Pro)	FCN3 (L160P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278378	NM_003665.4(FCN3):c.488T>A (p.Leu163Gln)	FCN3 (L152Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314800	NM_003665.4(FCN3):c.458G>A (p.Gly153Asp)	FCN3 (G142D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278377	NM_003665.4(FCN3):c.434G>A (p.Arg145His)	FCN3 (R145H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361621	NM_003665.4(FCN3):c.416G>A (p.Gly139Asp)	FCN3 (G128D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 813624	NM_003665.4(FCN3):c.386G>A (p.Gly129Asp)	FCN3 (G118D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094165	NM_003665.4(FCN3):c.385G>A (p.Gly129Ser)	FCN3 (G129S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550370	NM_003665.4(FCN3):c.305C>A (p.Thr102Asn)	FCN3 (T91N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458681	NM_003665.4(FCN3):c.254G>A (p.Arg85Gln)	FCN3 (R85Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494189	NM_003665.4(FCN3):c.233G>C (p.Gly78Ala)	FCN3 (G78A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094164	NM_003665.4(FCN3):c.209A>G (p.Lys70Arg)	FCN3 (K70R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464933	NM_003665.4(FCN3):c.142G>A (p.Gly48Arg)	FCN3 (G48R)	Single nucleotide variant (missense variant)	not specified +1 more	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: 22