"Ambry Genetics"[submitter] AND "ZNF773"[gene] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2399304	NM_198542.3(ZNF773):c.85T>G (p.Trp29Gly)	ZNF773 (W29G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198233	NM_198542.3(ZNF773):c.103G>A (p.Ala35Thr)	ZNF773 (A34T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2263638	NM_198542.3(ZNF773):c.103G>T (p.Ala35Ser)	ZNF773 (A34S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601865	NM_198542.3(ZNF773):c.111G>T (p.Arg37Ser)	ZNF773 (R36S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314763	NM_198542.3(ZNF773):c.125A>G (p.Asn42Ser)	ZNF773 (N41S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259487	NM_198542.3(ZNF773):c.146C>T (p.Thr49Ile)	ZNF773 (T49I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206086	NM_198542.3(ZNF773):c.158C>G (p.Ser53Cys)	ZNF773 (S53C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466224	NM_198542.3(ZNF773):c.178A>G (p.Lys60Glu)	ZNF773 (K60E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198234	NM_198542.3(ZNF773):c.257T>C (p.Leu86Pro)	ZNF773 (L85P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2287219	NM_198542.3(ZNF773):c.274G>C (p.Gly92Arg)	ZNF773 (K89N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198235	NM_198542.3(ZNF773):c.289G>A (p.Ala97Thr)	ZNF773 (A97T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2411395	NM_198542.3(ZNF773):c.308C>T (p.Ala103Val)	ZNF773 (L101F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265860	NM_198542.3(ZNF773):c.319G>A (p.Val107Met)	ZNF773 (V106M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2345515	NM_198542.3(ZNF773):c.320T>C (p.Val107Ala)	ZNF773 (V107A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198236	NM_198542.3(ZNF773):c.334G>A (p.Val112Ile)	ZNF773 (V112I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198237	NM_198542.3(ZNF773):c.355C>T (p.His119Tyr)	ZNF773 (H118Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198238	NM_198542.3(ZNF773):c.385G>A (p.Glu129Lys)	ZNF773 (E129K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2466225	NM_198542.3(ZNF773):c.385G>C (p.Glu129Gln)	ZNF773 (E128Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2338267	NM_198542.3(ZNF773):c.406A>T (p.Arg136Trp)	ZNF773 (R135W +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198239	NM_198542.3(ZNF773):c.422A>G (p.His141Arg)	ZNF773 (H140R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2485244	NM_198542.3(ZNF773):c.481G>T (p.Gly161Cys)	ZNF773 (G160C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2508612	NM_198542.3(ZNF773):c.514G>C (p.Glu172Gln)	ZNF773 (E172Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2537010	NM_198542.3(ZNF773):c.544G>C (p.Glu182Gln)	ZNF773 (E181Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2545946	NM_198542.3(ZNF773):c.550T>C (p.Phe184Leu)	ZNF773 (F184L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2541465	NM_198542.3(ZNF773):c.566G>A (p.Arg189Lys)	ZNF773 (R189K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198240	NM_198542.3(ZNF773):c.715A>G (p.Ile239Val)	ZNF773 (I238V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2603600	NM_198542.3(ZNF773):c.736C>T (p.Pro246Ser)	ZNF773 (P246S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3259486	NM_198542.3(ZNF773):c.777T>A (p.Asn259Lys)	ZNF773 (N259K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198241	NM_198542.3(ZNF773):c.802G>C (p.Val268Leu)	ZNF773 (V267L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2251181	NM_198542.3(ZNF773):c.814G>A (p.Glu272Lys)	ZNF773 (E272K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2209736	NM_198542.3(ZNF773):c.820C>T (p.Pro274Ser)	ZNF773 (P273S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2522464	NM_198542.3(ZNF773):c.829T>C (p.Cys277Arg)	ZNF773 (C277R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2278918	NM_198542.3(ZNF773):c.967A>G (p.Arg323Gly)	ZNF773 (R323G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3259485	NM_198542.3(ZNF773):c.970G>A (p.Val324Ile)	ZNF773 (V324I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3259488	NM_198542.3(ZNF773):c.1018T>C (p.Tyr340His)	ZNF773 (Y339H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2595319	NM_198542.3(ZNF773):c.1025A>G (p.His342Arg)	ZNF773 (H342R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2381895	NM_198542.3(ZNF773):c.1091G>A (p.Cys364Tyr)	ZNF773 (C364Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2399420	NM_198542.3(ZNF773):c.1133G>A (p.Arg378Gln)	ZNF773 (R377Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2591377	NM_198542.3(ZNF773):c.1185C>G (p.Phe395Leu)	ZNF773 (F395L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2590577	NM_198542.3(ZNF773):c.1300C>G (p.Arg434Gly)	ZNF773 (R434G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3259489	NM_198542.3(ZNF773):c.1312A>G (p.Thr438Ala)	ZNF773 (T438A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 41