"Ambry Genetics"[submitter] AND "FZD3"[gene] - ClinVar

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

Search results

Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3097672	NM_017412.4(FZD3):c.9G>T (p.Met3Ile)	FZD3 (M3I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2623450	NM_017412.4(FZD3):c.56A>G (p.His19Arg)	FZD3 (H19R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2254072	NM_017412.4(FZD3):c.118C>T (p.Pro40Ser)	FZD3 (P40S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280290	NM_017412.4(FZD3):c.136A>C (p.Met46Leu)	FZD3 (M46L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2294004	NM_017412.4(FZD3):c.137T>C (p.Met46Thr)	FZD3 (M46T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278912	NM_017412.4(FZD3):c.233G>A (p.Arg78Gln)	FZD3 (R101Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280287	NM_017412.4(FZD3):c.406C>T (p.Pro136Ser)	FZD3 (P75S +6 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2531367	NM_017412.4(FZD3):c.547C>T (p.Arg183Cys)	FZD3 (R206C +6 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2260798	NM_017412.4(FZD3):c.695G>A (p.Arg232His)	FZD3 (R170H +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214670	NM_017412.4(FZD3):c.794A>G (p.Asn265Ser)	FZD3 (N138S +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210068	NM_017412.4(FZD3):c.997G>A (p.Ala333Thr)	FZD3 (A142T +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097667	NM_017412.4(FZD3):c.1030A>G (p.Ile344Val)	FZD3 (I344V +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3280291	NM_017412.4(FZD3):c.1111T>G (p.Leu371Val)	FZD3 (L310V +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2509423	NM_017412.4(FZD3):c.1340G>A (p.Gly447Asp)	FZD3 (G170D +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3097669	NM_017412.4(FZD3):c.1421G>A (p.Arg474His)	FZD3 (R197H +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601701	NM_017412.4(FZD3):c.1571G>A (p.Arg524Gln)	FZD3 (R397Q +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486079	NM_017412.4(FZD3):c.1594T>G (p.Phe532Val)	FZD3 (F465V +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097670	NM_017412.4(FZD3):c.1625C>T (p.Thr542Ile)	FZD3 (T265I +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2603176	NM_017412.4(FZD3):c.1675C>T (p.His559Tyr)	FZD3 (H368Y +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3280288	NM_017412.4(FZD3):c.1724C>G (p.Ala575Gly)	FZD3 (A448G +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3280286	NM_017412.4(FZD3):c.1759G>A (p.Gly587Ser)	FZD3 (G116S +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534827	NM_017412.4(FZD3):c.1769A>G (p.His590Arg)	FZD3 (H119R +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097671	NM_017412.4(FZD3):c.1906A>G (p.Ser636Gly)	FZD3 (S636G +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3280289	NM_017412.4(FZD3):c.1933C>A (p.Pro645Thr)	FZD3 (P584T +9 more)	Single nucleotide variant (missense variant +1 more)	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: 24