"Ambry Genetics"[submitter] AND "FZD9"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2384720	NM_003508.3(FZD9):c.53C>T (p.Ala18Val)	FZD9 (A18V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611217	NM_003508.3(FZD9):c.106G>T (p.Ala36Ser)	FZD9 (A36S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259929	NM_003508.3(FZD9):c.305A>T (p.Asp102Val)	FZD9 (D102V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536057	NM_003508.3(FZD9):c.383A>C (p.Gln128Pro)	FZD9 (Q128P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237274	NM_003508.3(FZD9):c.447C>A (p.His149Gln)	FZD9 (H149Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458446	NM_003508.3(FZD9):c.566G>A (p.Gly189Asp)	FZD9 (G189D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097709	NM_003508.3(FZD9):c.589G>C (p.Glu197Gln)	FZD9 (E197Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097710	NM_003508.3(FZD9):c.772C>T (p.His258Tyr)	FZD9 (H258Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313643	NM_003508.3(FZD9):c.824A>G (p.Asn275Ser)	FZD9 (N275S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410789	NM_003508.3(FZD9):c.893C>T (p.Ala298Val)	FZD9 (A298V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097711	NM_003508.3(FZD9):c.965A>G (p.Tyr322Cys)	FZD9 (Y322C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340169	NM_003508.3(FZD9):c.1345G>C (p.Gly449Arg)	FZD9 (G449R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542865	NM_003508.3(FZD9):c.1364A>G (p.Tyr455Cys)	FZD9 (Y455C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228023	NM_003508.3(FZD9):c.1415A>G (p.Asn472Ser)	FZD9, LOC123956159 (N472S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472655	NM_003508.3(FZD9):c.1436G>A (p.Arg479Gln)	FZD9, LOC123956159 (R479Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266379	NM_003508.3(FZD9):c.1466C>T (p.Ala489Val)	FZD9, LOC123956159 (A489V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216298	NM_003508.3(FZD9):c.1484G>A (p.Arg495Lys)	FZD9, LOC123956159 (R495K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280310	NM_003508.3(FZD9):c.1519G>A (p.Val507Met)	FZD9, LOC123956159 (V507M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289599	NM_003508.3(FZD9):c.1541T>C (p.Ile514Thr)	FZD9, LOC123956159 (I514T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097708	NM_003508.3(FZD9):c.1636G>C (p.Ala546Pro)	FZD9, LOC123956159 (A546P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 20