UHRF2[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3186277	NM_152896.3(UHRF2):c.50A>G (p.Glu17Gly)	UHRF2 (E17G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2659060	NM_152896.3(UHRF2):c.255A>G (p.Thr85=)	UHRF2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3186272	NM_152896.3(UHRF2):c.278C>G (p.Ser93Cys)	UHRF2 (S93C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330902	NM_152896.3(UHRF2):c.308C>G (p.Pro103Arg)	UHRF2 (P103R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330901	NM_152896.3(UHRF2):c.311G>A (p.Arg104Lys)	UHRF2 (R104K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2287765	NM_152896.3(UHRF2):c.314T>C (p.Val105Ala)	UHRF2 (V105A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186274	NM_152896.3(UHRF2):c.338C>T (p.Thr113Ile)	UHRF2 (T113I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2217036	NM_152896.3(UHRF2):c.346C>T (p.Arg116Cys)	UHRF2 (R116C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186275	NM_152896.3(UHRF2):c.359T>C (p.Ile120Thr)	UHRF2 (I120T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397199	NM_152896.3(UHRF2):c.377T>C (p.Ile126Thr)	UHRF2 (I126T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273032	NM_152896.3(UHRF2):c.460G>T (p.Ala154Ser)	UHRF2 (A154S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186276	NM_152896.3(UHRF2):c.509C>A (p.Ser170Tyr)	UHRF2 (S170Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186278	NM_152896.3(UHRF2):c.551A>G (p.Glu184Gly)	UHRF2 (E184G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213989	NM_152896.3(UHRF2):c.559A>C (p.Asn187His)	UHRF2 (N187H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622441	NM_152896.3(UHRF2):c.619G>A (p.Val207Ile)	UHRF2 (V207I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330904	NM_152896.3(UHRF2):c.623T>C (p.Ile208Thr)	UHRF2 (I208T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330900	NM_152896.3(UHRF2):c.676G>A (p.Val226Ile)	UHRF2 (V226I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528944	NM_152896.3(UHRF2):c.786C>G (p.Phe262Leu)	UHRF2 (F262L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186279	NM_152896.3(UHRF2):c.844C>T (p.Arg282Cys)	UHRF2 (R282C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406110	NM_152896.3(UHRF2):c.977G>A (p.Arg326Gln)	UHRF2 (R326Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240954	NM_152896.3(UHRF2):c.1102G>T (p.Ala368Ser)	UHRF2 (A368S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602583	NM_152896.3(UHRF2):c.1106A>T (p.Tyr369Phe)	UHRF2 (Y369F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186270	NM_152896.3(UHRF2):c.1268G>A (p.Arg423Gln)	UHRF2 (R423Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558557	NM_152896.3(UHRF2):c.1976G>C (p.Ser659Thr)	UHRF2 (S659T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222869	NM_152896.3(UHRF2):c.2029G>T (p.Val677Leu)	UHRF2 (V677L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330903	NM_152896.3(UHRF2):c.2046T>G (p.Asp682Glu)	UHRF2 (D682E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186271	NM_152896.3(UHRF2):c.2048C>T (p.Ser683Leu)	UHRF2 (S683L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284248	NM_152896.3(UHRF2):c.2140C>G (p.Leu714Val)	UHRF2 (L714V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604761	NM_152896.3(UHRF2):c.2179T>A (p.Leu727Met)	UHRF2 (L727M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527380	NM_152896.3(UHRF2):c.2246T>G (p.Phe749Cys)	UHRF2 (F749C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321466	NM_152896.3(UHRF2):c.2357T>A (p.Ile786Asn)	UHRF2 (I786N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 31