"Ambry Genetics"[submitter] AND "FZD8"[gene] - ClinVar

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Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2283426	NM_031866.3(FZD8):c.2039C>G (p.Ala680Gly)	FZD8 (A680G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230450	NM_031866.3(FZD8):c.2036C>T (p.Thr679Met)	FZD8 (T679M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097704	NM_031866.3(FZD8):c.1964G>T (p.Gly655Val)	FZD8 (G655V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544424	NM_031866.3(FZD8):c.1945G>C (p.Gly649Arg)	FZD8 (G649R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342984	NM_031866.3(FZD8):c.1937G>A (p.Gly646Asp)	FZD8 (G646D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2313886	NM_031866.3(FZD8):c.1906A>G (p.Thr636Ala)	FZD8 (T636A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482619	NM_031866.3(FZD8):c.1891G>A (p.Gly631Arg)	FZD8 (G631R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591865	NM_031866.3(FZD8):c.1886T>G (p.Val629Gly)	FZD8 (V629G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260186	NM_031866.3(FZD8):c.1883C>T (p.Ala628Val)	FZD8 (A628V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299372	NM_031866.3(FZD8):c.1722G>T (p.Gln574His)	FZD8 (Q574H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410309	NM_031866.3(FZD8):c.1679G>A (p.Arg560His)	FZD8 (R560H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263310	NM_031866.3(FZD8):c.1505C>T (p.Ala502Val)	FZD8, LOC124403940 (A502V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280309	NM_031866.3(FZD8):c.1494G>A (p.Met498Ile)	FZD8, LOC124403940 (M498I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280307	NM_031866.3(FZD8):c.1439A>G (p.Asn480Ser)	FZD8, LOC124403940 (N480S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314828	NM_031866.3(FZD8):c.1298C>T (p.Ala433Val)	FZD8, LOC124403940 (A433V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097703	NM_031866.3(FZD8):c.1228A>G (p.Ser410Gly)	FZD8, LOC124403940 (S410G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242671	NM_031866.3(FZD8):c.1210T>A (p.Tyr404Asn)	FZD8 (Y404N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097702	NM_031866.3(FZD8):c.1108C>G (p.Pro370Ala)	FZD8 (P370A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556724	NM_031866.3(FZD8):c.1100C>T (p.Ala367Val)	FZD8 (A367V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382693	NM_031866.3(FZD8):c.1093G>C (p.Ala365Pro)	FZD8 (A365P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097701	NM_031866.3(FZD8):c.1088C>G (p.Ala363Gly)	FZD8 (A363G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209319	NM_031866.3(FZD8):c.1088C>T (p.Ala363Val)	FZD8 (A363V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329816	NM_031866.3(FZD8):c.817G>A (p.Glu273Lys)	FZD8, LOC130003691 (E273K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271041	NM_031866.3(FZD8):c.793C>T (p.His265Tyr)	FZD8, LOC130003691 (H265Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214905	NM_031866.3(FZD8):c.768G>C (p.Gln256His)	FZD8 (Q256H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392806	NM_031866.3(FZD8):c.707C>T (p.Ala236Val)	FZD8 (A236V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612419	NM_031866.3(FZD8):c.692G>A (p.Gly231Glu)	FZD8 (G231E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596317	NM_031866.3(FZD8):c.670G>C (p.Gly224Arg)	FZD8, LOC130003692 (G224R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493709	NM_031866.3(FZD8):c.661C>T (p.Pro221Ser)	FZD8, LOC130003692 (P221S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616606	NM_031866.3(FZD8):c.598G>A (p.Gly200Ser)	FZD8, LOC130003692 (G200S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365228	NM_031866.3(FZD8):c.595G>A (p.Gly199Ser)	FZD8, LOC130003692 (G199S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365836	NM_031866.3(FZD8):c.574C>T (p.His192Tyr)	FZD8 (H192Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314214	NM_031866.3(FZD8):c.572C>G (p.Pro191Arg)	FZD8 (P191R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346238	NM_031866.3(FZD8):c.568C>T (p.Pro190Ser)	FZD8 (P190S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097706	NM_031866.3(FZD8):c.566G>A (p.Arg189Lys)	FZD8 (R189K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621053	NM_031866.3(FZD8):c.556C>T (p.Pro186Ser)	FZD8 (P186S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280306	NM_031866.3(FZD8):c.530C>T (p.Pro177Leu)	FZD8 (P177L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557860	NM_031866.3(FZD8):c.518G>C (p.Gly173Ala)	FZD8 (G173A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483734	NM_031866.3(FZD8):c.488C>T (p.Pro163Leu)	FZD8 (P163L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097705	NM_031866.3(FZD8):c.347C>G (p.Ala116Gly)	FZD8 (A116G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621487	NM_031866.3(FZD8):c.322C>G (p.Arg108Gly)	FZD8 (R108G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466331	NM_031866.3(FZD8):c.167A>G (p.Gln56Arg)	FZD8 (Q56R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280308	NM_031866.3(FZD8):c.73G>C (p.Ala25Pro)	FZD8 (A25P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097707	NM_031866.3(FZD8):c.71G>A (p.Gly24Asp)	FZD8 (G24D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

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Items: 44