"Ambry Genetics"[submitter] AND "ZBTB41"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3333952	NM_194314.3(ZBTB41):c.2577A>C (p.Lys859Asn)	ZBTB41 (K859N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461086	NM_194314.3(ZBTB41):c.2573A>G (p.Glu858Gly)	ZBTB41 (E858G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3333953	NM_194314.3(ZBTB41):c.2525A>G (p.Gln842Arg)	ZBTB41 (Q842R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463816	NM_194314.3(ZBTB41):c.2476C>T (p.Arg826Cys)	ZBTB41 (R826C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3333949	NM_194314.3(ZBTB41):c.2399A>C (p.Gln800Pro)	ZBTB41 (Q800P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343052	NM_194314.3(ZBTB41):c.2264C>G (p.Pro755Arg)	ZBTB41 (P755R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619480	NM_194314.3(ZBTB41):c.2247A>G (p.Ile749Met)	ZBTB41 (I749M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619272	NM_194314.3(ZBTB41):c.2203C>T (p.Arg735Trp)	ZBTB41 (R735W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528013	NM_194314.3(ZBTB41):c.1973A>G (p.Lys658Arg)	ZBTB41 (K658R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548303	NM_194314.3(ZBTB41):c.1760G>T (p.Gly587Val)	ZBTB41 (G587V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192080	NM_194314.3(ZBTB41):c.1610T>G (p.Ile537Arg)	ZBTB41 (I537R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488658	NM_194314.3(ZBTB41):c.1609A>G (p.Ile537Val)	ZBTB41 (I537V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601426	NM_194314.3(ZBTB41):c.1574G>A (p.Arg525His)	ZBTB41 (R525H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494473	NM_194314.3(ZBTB41):c.1489G>A (p.Glu497Lys)	ZBTB41 (E497K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205331	NM_194314.3(ZBTB41):c.1307C>A (p.Thr436Asn)	ZBTB41 (T436N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3333950	NM_194314.3(ZBTB41):c.1282A>G (p.Asn428Asp)	ZBTB41 (N428D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298457	NM_194314.3(ZBTB41):c.1189C>T (p.Arg397Cys)	ZBTB41 (R397C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192079	NM_194314.3(ZBTB41):c.1174G>A (p.Asp392Asn)	ZBTB41 (D392N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367035	NM_194314.3(ZBTB41):c.1027A>C (p.Asn343His)	ZBTB41 (N343H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192081	NM_194314.3(ZBTB41):c.856G>C (p.Asp286His)	ZBTB41 (D286H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541988	NM_194314.3(ZBTB41):c.833A>C (p.Asp278Ala)	ZBTB41 (D278A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597094	NM_194314.3(ZBTB41):c.707G>A (p.Gly236Glu)	ZBTB41 (G236E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3333948	NM_194314.3(ZBTB41):c.692G>A (p.Arg231Lys)	ZBTB41 (R231K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394029	NM_194314.3(ZBTB41):c.637A>G (p.Ser213Gly)	ZBTB41 (S213G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354685	NM_194314.3(ZBTB41):c.617A>G (p.Asn206Ser)	ZBTB41 (N206S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374854	NM_194314.3(ZBTB41):c.593A>G (p.Glu198Gly)	ZBTB41 (E198G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377769	NM_194314.3(ZBTB41):c.560C>T (p.Thr187Ile)	ZBTB41 (T187I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596364	NM_194314.3(ZBTB41):c.559A>C (p.Thr187Pro)	ZBTB41 (T187P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256205	NM_194314.3(ZBTB41):c.391G>A (p.Val131Ile)	ZBTB41 (V131I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597881	NM_194314.3(ZBTB41):c.356A>G (p.Lys119Arg)	ZBTB41 (K119R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369362	NM_194314.3(ZBTB41):c.159A>T (p.Glu53Asp)	ZBTB41 (E53D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492006	NM_194314.3(ZBTB41):c.155A>C (p.Gln52Pro)	ZBTB41 (Q52P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360479	NM_194314.3(ZBTB41):c.124A>G (p.Arg42Gly)	ZBTB41 (R42G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247738	NM_194314.3(ZBTB41):c.55C>G (p.His19Asp)	ZBTB41 (H19D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 34